rs3101942

Variant names:

• chr6-32902280-G-A
• rs3101942
• ENST00000685247.3:n.2244G>A

Your query was ambiguous. Multiple possible variants found:

• chr6-32902280-G-A
• chr6-32902280-G-C
• chr6-32902280-G-T

Variant summary

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

The NR_037177.1(LOC100294145):​n.2212G>A 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 0.67 in 152,010 control chromosomes in the GnomAD database, including 35,439 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 0.67 (35439 hom., cov: 32)
• Consequence: LOC100294145 NR_037177.1 non_coding_transcript_exon
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.687
• Publications: 37 publications found

Genes affected

ENSG00000289047 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.87 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NR_037177.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LOC100294145	NR_037177.1		n.2212G>A		non_coding_transcript_exon	Exon 2 of 2
	LOC100294145	NR_037178.1		n.2113G>A		non_coding_transcript_exon	Exon 2 of 2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000289047	ENST00000685247.3		n.2244G>A		non_coding_transcript_exon	Exon 2 of 2
	ENSG00000289047	ENST00000701517.2		n.2044G>A		non_coding_transcript_exon	Exon 2 of 2
	ENSG00000289047	ENST00000753208.1		n.1881G>A		non_coding_transcript_exon	Exon 2 of 2

Frequencies

GnomAD3 genomes AF: 0.669 AC: 101686 AN: 151892 Hom.: 35381 Cov.: 32

Gnomad AFR AF: 0.877

Gnomad AMI AF: 0.577

Gnomad AMR AF: 0.628

Gnomad ASJ AF: 0.546

Gnomad EAS AF: 0.615

Gnomad SAS AF: 0.576

Gnomad FIN AF: 0.534

Gnomad MID AF: 0.653

Gnomad NFE AF: 0.591

Gnomad OTH AF: 0.696

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

GnomAD4 genome AF: 0.670 AC: 101801 AN: 152010 Hom.: 35439 Cov.: 32 AF XY: 0.662 AC XY: 49139 AN XY: 74270

African (AFR) AF: 0.877 AC: 36425 AN: 41516

American (AMR) AF: 0.628 AC: 9587 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.546 AC: 1893 AN: 3464

East Asian (EAS) AF: 0.616 AC: 3185 AN: 5172

South Asian (SAS) AF: 0.576 AC: 2778 AN: 4824

European-Finnish (FIN) AF: 0.534 AC: 5611 AN: 10512

Middle Eastern (MID) AF: 0.658 AC: 192 AN: 292

European-Non Finnish (NFE) AF: 0.591 AC: 40137 AN: 67930

Other (OTH) AF: 0.694 AC: 1467 AN: 2114

Alfa AF: 0.646 Hom.: 54870

Bravo AF: 0.688

Asia WGS AF: 0.616 AC: 2132 AN: 3460

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	0.12
DANN	Benign	0.81
PhyloP100		-0.69

Splicing

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

Other links and lift over

dbSNP: rs3101942; hg19: chr6-32870057;