chr3-47414198-C-T
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Variant summary
Our verdict is Benign. Variant got -9 ACMG points: 0P and 9B. BP4_ModerateBP6_ModerateBP7BS2
The NM_012235.4(SCAP):c.3576G>A(p.Lys1192=) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00592 in 1,613,752 control chromosomes in the GnomAD database, including 42 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).
Frequency
Genomes: 𝑓 0.0045 ( 4 hom., cov: 33)
Exomes 𝑓: 0.0061 ( 38 hom. )
Consequence
SCAP
NM_012235.4 synonymous
NM_012235.4 synonymous
Scores
2
Clinical Significance
Conservation
PhyloP100: 0.719
Genes affected
SCAP (HGNC:30634): (SREBF chaperone) This gene encodes a protein with a sterol sensing domain (SSD) and seven WD domains. In the presence of cholesterol, this protein binds to sterol regulatory element binding proteins (SREBPs) and mediates their transport from the ER to the Golgi. The SREBPs are then proteolytically cleaved and regulate sterol biosynthesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
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ACMG classification
Classification made for transcript
Verdict is Benign. Variant got -9 ACMG points.
BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.43).
BP6
Variant 3-47414198-C-T is Benign according to our data. Variant chr3-47414198-C-T is described in ClinVar as [Benign]. Clinvar id is 777773.Status of the report is criteria_provided_single_submitter, 1 stars.
BP7
Synonymous conserved (PhyloP=0.719 with no splicing effect.
BS2
High Homozygotes in GnomAd4 at 4 AR gene
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
SCAP | NM_012235.4 | c.3576G>A | p.Lys1192= | synonymous_variant | 22/23 | ENST00000265565.10 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
SCAP | ENST00000265565.10 | c.3576G>A | p.Lys1192= | synonymous_variant | 22/23 | 1 | NM_012235.4 | P1 | |
SCAP | ENST00000648151.1 | c.3576G>A | p.Lys1192= | synonymous_variant | 23/24 | P1 | |||
SCAP | ENST00000320017.10 | c.*2290G>A | 3_prime_UTR_variant, NMD_transcript_variant | 17/18 | 2 | ||||
SCAP | ENST00000441517.6 | c.*2722G>A | 3_prime_UTR_variant, NMD_transcript_variant | 19/20 | 2 |
Frequencies
GnomAD3 genomes AF: 0.00454 AC: 691AN: 152208Hom.: 4 Cov.: 33
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GnomAD3 exomes AF: 0.00434 AC: 1089AN: 250708Hom.: 3 AF XY: 0.00443 AC XY: 601AN XY: 135656
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GnomAD4 exome AF: 0.00606 AC: 8863AN: 1461426Hom.: 38 Cov.: 32 AF XY: 0.00590 AC XY: 4286AN XY: 726988
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GnomAD4 genome AF: 0.00454 AC: 691AN: 152326Hom.: 4 Cov.: 33 AF XY: 0.00466 AC XY: 347AN XY: 74478
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ClinVar
Significance: Benign
Submissions summary: Benign:1
Revision: criteria provided, single submitter
LINK: link
Submissions by phenotype
not provided Benign:1
Benign, criteria provided, single submitter | clinical testing | Invitae | Dec 07, 2017 | - - |
Computational scores
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BayesDel_noAF
Benign
CADD
Benign
DANN
Benign
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Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at