6-159521923-G-A

Variant names:

• chr6-159521923-G-A
• rs12197995
• ENST00000656085.1:n.43-52408C>T

Variant summary

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

The ENST00000656085.1(ENSG00000286533):​n.43-52408C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.272 in 152,022 control chromosomes in the GnomAD database, including 6,811 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 0.27 (6811 hom., cov: 31)
• Consequence: ENSG00000286533 ENST00000656085.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.609
• Publications: 5 publications found

Genes affected

ENSG00000286533 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.79).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.378 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000656085.1. 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
	ENSG00000286533	ENST00000656085.1		n.43-52408C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.272 AC: 41321 AN: 151902 Hom.: 6814 Cov.: 31

Gnomad AFR AF: 0.109

Gnomad AMI AF: 0.305

Gnomad AMR AF: 0.246

Gnomad ASJ AF: 0.414

Gnomad EAS AF: 0.0280

Gnomad SAS AF: 0.310

Gnomad FIN AF: 0.287

Gnomad MID AF: 0.347

Gnomad NFE AF: 0.382

Gnomad OTH AF: 0.293

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

GnomAD4 genome AF: 0.272 AC: 41316 AN: 152022 Hom.: 6811 Cov.: 31 AF XY: 0.268 AC XY: 19942 AN XY: 74322

African (AFR) AF: 0.108 AC: 4494 AN: 41488

American (AMR) AF: 0.245 AC: 3750 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.414 AC: 1438 AN: 3470

East Asian (EAS) AF: 0.0281 AC: 145 AN: 5164

South Asian (SAS) AF: 0.311 AC: 1491 AN: 4798

European-Finnish (FIN) AF: 0.287 AC: 3030 AN: 10556

Middle Eastern (MID) AF: 0.344 AC: 101 AN: 294

European-Non Finnish (NFE) AF: 0.382 AC: 25980 AN: 67954

Other (OTH) AF: 0.289 AC: 609 AN: 2106

Alfa AF: 0.345 Hom.: 10337

Bravo AF: 0.257

Asia WGS AF: 0.174 AC: 605 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.79
CADD	Benign	6.4
DANN	Benign	0.88
PhyloP100		-0.61

Splicing

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

Other links and lift over

dbSNP: rs12197995; hg19: chr6-159942955; COSMIC: COSV68549806;