chr6-83710074-G-A

Variant names:

• chr6-83710074-G-A
• rs624076
• ENST00000443471.3:n.141+355G>A

Variant summary

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

The ENST00000443471.3(ENSG00000237874):​n.141+355G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.319 in 151,812 control chromosomes in the GnomAD database, including 10,872 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 0.32 (10872 hom., cov: 32)
• Consequence: ENSG00000237874 ENST00000443471.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.306
• Publications: 6 publications found

Genes affected

ENSG00000237874 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.634 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000443471.3. 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
	LOC105377879	NR_136251.1		n.278+355G>A		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000237874	ENST00000443471.3	TSL:3	n.141+355G>A		intron	N/A
	ENSG00000237874	ENST00000781263.1		n.289+355G>A		intron	N/A
	ENSG00000237874	ENST00000781264.1		n.253+355G>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.319 AC: 48365 AN: 151694 Hom.: 10828 Cov.: 32

Gnomad AFR AF: 0.640

Gnomad AMI AF: 0.191

Gnomad AMR AF: 0.228

Gnomad ASJ AF: 0.249

Gnomad EAS AF: 0.267

Gnomad SAS AF: 0.279

Gnomad FIN AF: 0.121

Gnomad MID AF: 0.307

Gnomad NFE AF: 0.187

Gnomad OTH AF: 0.312

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

GnomAD4 genome AF: 0.319 AC: 48463 AN: 151812 Hom.: 10872 Cov.: 32 AF XY: 0.315 AC XY: 23326 AN XY: 74154

African (AFR) AF: 0.640 AC: 26503 AN: 41392

American (AMR) AF: 0.228 AC: 3477 AN: 15250

Ashkenazi Jewish (ASJ) AF: 0.249 AC: 864 AN: 3470

East Asian (EAS) AF: 0.267 AC: 1370 AN: 5130

South Asian (SAS) AF: 0.278 AC: 1335 AN: 4802

European-Finnish (FIN) AF: 0.121 AC: 1276 AN: 10532

Middle Eastern (MID) AF: 0.316 AC: 93 AN: 294

European-Non Finnish (NFE) AF: 0.187 AC: 12711 AN: 67930

Other (OTH) AF: 0.314 AC: 661 AN: 2106

Alfa AF: 0.232 Hom.: 6635

Bravo AF: 0.339

Asia WGS AF: 0.322 AC: 1125 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	1.3
DANN	Benign	0.79
PhyloP100		-0.31
PromoterAI		-0.0082	Neutral

Splicing

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

Other links and lift over

dbSNP: rs624076; hg19: chr6-84419793; COSMIC: COSV52132688;