7-74068657-G-A

Variant summary

Our verdict is Benign. The variant received -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBS1BS2

The NM_000501.4(ELN):​c.2132G>A​(p.Gly711Asp) variant causes a missense, splice region change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00425 in 1,614,152 control chromosomes in the GnomAD database, including 17 homozygotes. In-silico tool predicts a benign outcome for this variant. 3/3 splice prediction tools predict no significant impact on normal splicing. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.0032 ( 0 hom., cov: 32)
Exomes 𝑓: 0.0044 ( 17 hom. )

Consequence

ELN
NM_000501.4 missense, splice_region

Scores

2
6
10
Splicing: ADA: 0.006857
2

Clinical Significance

Benign/Likely benign criteria provided, multiple submitters, no conflicts B:13

Conservation

PhyloP100: 1.05

Publications

29 publications found
Variant links:
Genes affected
ELN (HGNC:3327): (elastin) This gene encodes a protein that is one of the two components of elastic fibers. Elastic fibers comprise part of the extracellular matrix and confer elasticity to organs and tissues including the heart, skin, lungs, ligaments, and blood vessels. The encoded protein is rich in hydrophobic amino acids such as glycine and proline, which form mobile hydrophobic regions bounded by crosslinks between lysine residues. Degradation products of the encoded protein, known as elastin-derived peptides or elastokines, bind the elastin receptor complex and other receptors and stimulate migration and proliferation of monocytes and skin fibroblasts. Elastokines can also contribute to cancer progression. Deletions and mutations in this gene are associated with supravalvular aortic stenosis (SVAS) and autosomal dominant cutis laxa. [provided by RefSeq, Aug 2017]
ELN Gene-Disease associations (from GenCC):
  • cutis laxa, autosomal dominant 1
    Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Labcorp Genetics (formerly Invitae), PanelApp Australia, Ambry Genetics, Genomics England PanelApp, G2P
  • supravalvular aortic stenosis
    Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Ambry Genetics, Orphanet, Labcorp Genetics (formerly Invitae)
  • autosomal dominant cutis laxa
    Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
  • familial thoracic aortic aneurysm and aortic dissection
    Inheritance: AD Classification: LIMITED Submitted by: Ambry Genetics

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ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -20 ACMG points.

BP4
Computational evidence support a benign effect (MetaRNN=0.011181653).
BP6
Variant 7-74068657-G-A is Benign according to our data. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-74068657-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 43585.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
BS1
Variant frequency is greater than expected in population amr. GnomAd4 allele frequency = 0.00316 (481/152288) while in subpopulation AMR AF = 0.00562 (86/15290). AF 95% confidence interval is 0.00466. There are 0 homozygotes in GnomAd4. There are 225 alleles in the male GnomAd4 subpopulation. Median coverage is 32. This position passed quality control check.
BS2
High AC in GnomAd4 at 481 AD gene.

Transcripts

RefSeq

Gene Transcript HGVSc HGVSp Effect Exon rank MANE Protein UniProt
ELNNM_000501.4 linkc.2132G>A p.Gly711Asp missense_variant, splice_region_variant Exon 33 of 33 ENST00000252034.12 NP_000492.2 P15502-2

Ensembl

Gene Transcript HGVSc HGVSp Effect Exon rank TSL MANE Protein Appris UniProt
ELNENST00000252034.12 linkc.2132G>A p.Gly711Asp missense_variant, splice_region_variant Exon 33 of 33 1 NM_000501.4 ENSP00000252034.7 P15502-2

Frequencies

GnomAD3 genomes
AF:
0.00316
AC:
481
AN:
152170
Hom.:
0
Cov.:
32
show subpopulations
Gnomad AFR
AF:
0.000941
Gnomad AMI
AF:
0.00
Gnomad AMR
AF:
0.00563
Gnomad ASJ
AF:
0.000576
Gnomad EAS
AF:
0.00
Gnomad SAS
AF:
0.000207
Gnomad FIN
AF:
0.00
Gnomad MID
AF:
0.00316
Gnomad NFE
AF:
0.00497
Gnomad OTH
AF:
0.00670
GnomAD2 exomes
AF:
0.00305
AC:
765
AN:
251040
AF XY:
0.00287
show subpopulations
Gnomad AFR exome
AF:
0.000554
Gnomad AMR exome
AF:
0.00480
Gnomad ASJ exome
AF:
0.000397
Gnomad EAS exome
AF:
0.00
Gnomad FIN exome
AF:
0.0000924
Gnomad NFE exome
AF:
0.00498
Gnomad OTH exome
AF:
0.00326
GnomAD4 exome
AF:
0.00436
AC:
6380
AN:
1461864
Hom.:
17
Cov.:
31
AF XY:
0.00417
AC XY:
3032
AN XY:
727240
show subpopulations
African (AFR)
AF:
0.000836
AC:
28
AN:
33480
American (AMR)
AF:
0.00519
AC:
232
AN:
44720
Ashkenazi Jewish (ASJ)
AF:
0.000497
AC:
13
AN:
26136
East Asian (EAS)
AF:
0.00
AC:
0
AN:
39700
South Asian (SAS)
AF:
0.00
AC:
0
AN:
86258
European-Finnish (FIN)
AF:
0.000131
AC:
7
AN:
53410
Middle Eastern (MID)
AF:
0.00191
AC:
11
AN:
5768
European-Non Finnish (NFE)
AF:
0.00527
AC:
5862
AN:
1111996
Other (OTH)
AF:
0.00376
AC:
227
AN:
60396
Allele Balance Distribution
Red line indicates average allele balance
Average allele balance: 0.469
Heterozygous variant carriers
0
352
704
1055
1407
1759
0.00
0.20
0.40
0.60
0.80
0.95
Allele balance

Age Distribution

Exome Het
Exome Hom
Variant carriers
0
226
452
678
904
1130
<30
30-35
35-40
40-45
45-50
50-55
55-60
60-65
65-70
70-75
75-80
>80
Age
GnomAD4 genome
AF:
0.00316
AC:
481
AN:
152288
Hom.:
0
Cov.:
32
AF XY:
0.00302
AC XY:
225
AN XY:
74450
show subpopulations
African (AFR)
AF:
0.000938
AC:
39
AN:
41560
American (AMR)
AF:
0.00562
AC:
86
AN:
15290
Ashkenazi Jewish (ASJ)
AF:
0.000576
AC:
2
AN:
3470
East Asian (EAS)
AF:
0.00
AC:
0
AN:
5174
South Asian (SAS)
AF:
0.000207
AC:
1
AN:
4832
European-Finnish (FIN)
AF:
0.00
AC:
0
AN:
10618
Middle Eastern (MID)
AF:
0.00340
AC:
1
AN:
294
European-Non Finnish (NFE)
AF:
0.00497
AC:
338
AN:
68026
Other (OTH)
AF:
0.00663
AC:
14
AN:
2112
Allele Balance Distribution
Red line indicates average allele balance
Average allele balance: 0.502
Heterozygous variant carriers
0
23
45
68
90
113
0.00
0.20
0.40
0.60
0.80
0.95
Allele balance

Age Distribution

Genome Het
Variant carriers
0
10
20
30
40
50
<30
30-35
35-40
40-45
45-50
50-55
55-60
60-65
65-70
70-75
75-80
>80
Age
Alfa
AF:
0.00409
Hom.:
4
Bravo
AF:
0.00352
TwinsUK
AF:
0.00512
AC:
19
ALSPAC
AF:
0.00571
AC:
22
ESP6500AA
AF:
0.000227
AC:
1
ESP6500EA
AF:
0.00395
AC:
34
ExAC
AF:
0.00287
AC:
349
Asia WGS
AF:
0.000577
AC:
2
AN:
3478
EpiCase
AF:
0.00485
EpiControl
AF:
0.00516

ClinVar

Significance: Benign/Likely benign
Submissions summary: Benign:13
Revision: criteria provided, multiple submitters, no conflicts
LINK: link

Submissions by phenotype

not provided Benign:5
-
Breakthrough Genomics, Breakthrough Genomics
Significance:Likely benign
Review Status:criteria provided, single submitter
Collection Method:not provided

- -

-
Genome Diagnostics Laboratory, Amsterdam University Medical Center
Significance:Likely benign
Review Status:no assertion criteria provided
Collection Method:clinical testing

- -

Mar 09, 2021
GeneDx
Significance:Likely benign
Review Status:criteria provided, single submitter
Collection Method:clinical testing

This variant is associated with the following publications: (PMID: 16374472, 16081882, 19029017, 28146470) -

-
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen
Significance:Likely benign
Review Status:no assertion criteria provided
Collection Method:clinical testing

- -

Apr 01, 2025
CeGaT Center for Human Genetics Tuebingen
Significance:Benign
Review Status:criteria provided, single submitter
Collection Method:clinical testing

ELN: BS1, BS2 -

not specified Benign:4
-
Genome Diagnostics Laboratory, University Medical Center Utrecht
Significance:Benign
Review Status:no assertion criteria provided
Collection Method:clinical testing

- -

-
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+
Significance:Benign
Review Status:no assertion criteria provided
Collection Method:clinical testing

- -

Jul 19, 2012
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine
Significance:Likely benign
Review Status:criteria provided, single submitter
Collection Method:clinical testing

Gly711Asp in exon 33 of ELN: This variant is not expected to have clinical signi ficance because it has been identified in 0.4% (34/8600) of European American ch romosomes from a broad population by the NHLBI Exome Sequencing Project (http:// evs.gs.washington.edu/EVS) and in 2.5% (5/196) of Tuscan (Italian) chromosomes f rom a broad population by the 1000 Genomes project (dbSNP rs41511151). Gly711A sp in exon 33 of ELN (rs41511151; allele frequency = 0.4%, 34/8600) ** -

Apr 09, 2025
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute
Significance:Likely benign
Review Status:criteria provided, single submitter
Collection Method:clinical testing

- -

Supravalvar aortic stenosis Benign:3
Jan 29, 2025
Labcorp Genetics (formerly Invitae), Labcorp
Significance:Likely benign
Review Status:criteria provided, single submitter
Collection Method:clinical testing

- -

Jun 14, 2016
Illumina Laboratory Services, Illumina
Significance:Likely benign
Review Status:criteria provided, single submitter
Collection Method:clinical testing

- -

May 28, 2019
Mendelics
Significance:Benign
Review Status:criteria provided, single submitter
Collection Method:clinical testing

- -

Cutis laxa, autosomal dominant Benign:1
Jun 14, 2016
Illumina Laboratory Services, Illumina
Significance:Likely benign
Review Status:criteria provided, single submitter
Collection Method:clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction
AlphaMissense
Pathogenic
0.64
BayesDel_addAF
Benign
-0.23
T
BayesDel_noAF
Benign
-0.10
CADD
Benign
17
DANN
Benign
0.97
DEOGEN2
Benign
0.13
T;T;.;T;T;.;.;.;.;T;.;.;.;.;.
Eigen
Uncertain
0.51
Eigen_PC
Uncertain
0.26
FATHMM_MKL
Uncertain
0.83
D
LIST_S2
Benign
0.69
T;T;T;T;T;T;T;T;T;T;T;T;T;T;T
MetaRNN
Benign
0.011
T;T;T;T;T;T;T;T;T;T;T;T;T;T;T
MetaSVM
Benign
-0.67
T
MutationAssessor
Benign
1.6
.;.;.;L;.;.;.;.;.;.;.;.;.;.;.
PhyloP100
1.0
PrimateAI
Uncertain
0.64
T
PROVEAN
Benign
-2.0
N;.;D;.;D;D;D;N;N;D;N;N;N;D;D
REVEL
Uncertain
0.34
Sift
Pathogenic
0.0
D;.;D;.;D;D;.;D;D;D;T;D;.;D;D
Sift4G
Uncertain
0.0030
D;D;D;D;D;D;D;D;D;D;D;D;D;D;D
Polyphen
0.99
D;D;D;.;D;D;D;D;D;D;D;D;D;D;.
Vest4
0.51
MVP
0.82
MPC
0.24
ClinPred
0.045
T
GERP RS
2.6
Varity_R
0.069
gMVP
0.39
Mutation Taster
=69/31
polymorphism

Splicing

Name
Calibrated prediction
Score
Prediction
dbscSNV1_ADA
Benign
0.0069
dbscSNV1_RF
Benign
0.17
SpliceAI score (max)
0.090
Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

Other links and lift over

dbSNP: rs41511151; hg19: chr7-73482987; API