ENST00000638964.1:n.484+81199T>C

Variant names:

• chr7-12883931-T-C
• rs6460985
• ENST00000638964.1:n.484+81199T>C

Variant summary

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

The ENST00000638964.1(ENSG00000229618):​n.484+81199T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.56 in 151,728 control chromosomes in the GnomAD database, including 24,950 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 0.56 (24950 hom., cov: 30)
• Consequence: ENSG00000229618 ENST00000638964.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.92
• Publications: 0 publications found

Genes affected

ENSG00000229618 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.758 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000638964.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000229618	ENST00000638964.1	TSL:5	n.484+81199T>C		intron	N/A
	ENSG00000229618	ENST00000639998.1	TSL:5	n.483+125615T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.560 AC: 84853 AN: 151610 Hom.: 24918 Cov.: 30

Gnomad AFR AF: 0.765

Gnomad AMI AF: 0.280

Gnomad AMR AF: 0.507

Gnomad ASJ AF: 0.453

Gnomad EAS AF: 0.491

Gnomad SAS AF: 0.467

Gnomad FIN AF: 0.519

Gnomad MID AF: 0.617

Gnomad NFE AF: 0.474

Gnomad OTH AF: 0.558

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.560 AC: 84920 AN: 151728 Hom.: 24950 Cov.: 30 AF XY: 0.561 AC XY: 41578 AN XY: 74100

African (AFR) AF: 0.765 AC: 31676 AN: 41410

American (AMR) AF: 0.506 AC: 7708 AN: 15226

Ashkenazi Jewish (ASJ) AF: 0.453 AC: 1571 AN: 3468

East Asian (EAS) AF: 0.490 AC: 2520 AN: 5140

South Asian (SAS) AF: 0.467 AC: 2251 AN: 4816

European-Finnish (FIN) AF: 0.519 AC: 5427 AN: 10456

Middle Eastern (MID) AF: 0.616 AC: 181 AN: 294

European-Non Finnish (NFE) AF: 0.474 AC: 32164 AN: 67900

Other (OTH) AF: 0.554 AC: 1167 AN: 2108

Alfa AF: 0.513 Hom.: 2492

Bravo AF: 0.565

Asia WGS AF: 0.523 AC: 1816 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.35
DANN	Benign	0.52
PhyloP100		-1.9

Splicing

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

Other links and lift over

dbSNP: rs6460985; hg19: chr7-12923556;