rs10516842

Variant names:

• chr4-89685029-A-G
• rs10516842
• ENST00000612706.2:n.773A>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000612706.2(ENSG00000251095):​n.773A>G variant causes a non coding transcript exon change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0556 in 152,162 control chromosomes in the GnomAD database, including 447 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.056 (447 hom., cov: 32)
  • Failed GnomAD Quality Control
• Consequence: ENSG00000251095 ENST00000612706.2 non_coding_transcript_exon
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.143
• Publications: 1 publications found

Genes affected

ENSG00000251095 (HGNC:):

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.128 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LOC124900602	XR_001741764.2	n.3525A>G		non_coding_transcript_exon_variant	Exon 1 of 3
LOC124900602	XR_007058465.1	n.3525A>G		non_coding_transcript_exon_variant	Exon 1 of 2
LOC124900602	XR_007058466.1	n.3525A>G		non_coding_transcript_exon_variant	Exon 1 of 3
LOC124900602	XR_938983.2	n.3525A>G		non_coding_transcript_exon_variant	Exon 1 of 3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ENSG00000251095	ENST00000612706.2	n.773A>G		non_coding_transcript_exon_variant	Exon 2 of 2	5
ENSG00000251095	ENST00000506864.5	n.472-6256A>G		intron_variant	Intron 3 of 3	4
ENSG00000251095	ENST00000507916.6	n.135-6256A>G		intron_variant	Intron 1 of 2	3

Frequencies

GnomAD3 genomes AF: 0.0554 AC: 8423 AN: 152046 Hom.: 438 Cov.: 32

Gnomad AFR AF: 0.130

Gnomad AMI AF: 0.0110

Gnomad AMR AF: 0.0259

Gnomad ASJ AF: 0.00231

Gnomad EAS AF: 0.0574

Gnomad SAS AF: 0.0311

Gnomad FIN AF: 0.0528

Gnomad MID AF: 0.0411

Gnomad NFE AF: 0.0223

Gnomad OTH AF: 0.0416

GnomAD4 exome Data not reliable, filtered out with message: AC0 AC: 0 AN: 0 Hom.: 0 Cov.: 0 AC XY: 0 AN XY: 0

African (AFR) AC: 0 AN: 0

American (AMR) AC: 0 AN: 0

Ashkenazi Jewish (ASJ) AC: 0 AN: 0

East Asian (EAS) AC: 0 AN: 0

South Asian (SAS) AC: 0 AN: 0

European-Finnish (FIN) AC: 0 AN: 0

Middle Eastern (MID) AC: 0 AN: 0

European-Non Finnish (NFE) AC: 0 AN: 0

Other (OTH) AC: 0 AN: 0

GnomAD4 genome AF: 0.0556 AC: 8463 AN: 152162 Hom.: 447 Cov.: 32 AF XY: 0.0556 AC XY: 4138 AN XY: 74408

African (AFR) AF: 0.130 AC: 5414 AN: 41512

American (AMR) AF: 0.0258 AC: 395 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.00231 AC: 8 AN: 3470

East Asian (EAS) AF: 0.0578 AC: 298 AN: 5160

South Asian (SAS) AF: 0.0307 AC: 148 AN: 4814

European-Finnish (FIN) AF: 0.0528 AC: 560 AN: 10608

Middle Eastern (MID) AF: 0.0476 AC: 14 AN: 294

European-Non Finnish (NFE) AF: 0.0223 AC: 1517 AN: 67984

Other (OTH) AF: 0.0468 AC: 99 AN: 2114

Alfa AF: 0.0381 Hom.: 105

Bravo AF: 0.0577

Asia WGS AF: 0.0700 AC: 243 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	1.7
DANN	Benign	0.67
PhyloP100		-0.14
Mutation Taster		=100/0	polymorphism

Splicing

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

Other links and lift over

dbSNP: rs10516842; hg19: chr4-90606180;