1-157939735-C-T

Variant names:

• chr1-157939735-C-T
• rs1925035
• ENST00000422062.1:n.262-2929C>T

Variant summary

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

The ENST00000422062.1(ENSG00000291226):​n.262-2929C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.324 in 152,006 control chromosomes in the GnomAD database, including 9,064 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 (9064 hom., cov: 31)
• Consequence: ENSG00000291226 ENST00000422062.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.297
• Publications: 3 publications found

Genes affected

ENSG00000291226 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.559 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000422062.1. 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
	LOC105371458	NR_135760.1		n.340-5921C>T		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000291226	ENST00000422062.1	TSL:2	n.262-2929C>T		intron	N/A
	ENSG00000291226	ENST00000452528.5	TSL:2	n.333-5921C>T		intron	N/A
	ENSG00000291226	ENST00000789662.1		n.342-5921C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.324 AC: 49169 AN: 151888 Hom.: 9051 Cov.: 31

Gnomad AFR AF: 0.153

Gnomad AMI AF: 0.264

Gnomad AMR AF: 0.475

Gnomad ASJ AF: 0.339

Gnomad EAS AF: 0.577

Gnomad SAS AF: 0.383

Gnomad FIN AF: 0.375

Gnomad MID AF: 0.283

Gnomad NFE AF: 0.362

Gnomad OTH AF: 0.355

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

GnomAD4 genome AF: 0.324 AC: 49181 AN: 152006 Hom.: 9064 Cov.: 31 AF XY: 0.329 AC XY: 24435 AN XY: 74296

African (AFR) AF: 0.153 AC: 6349 AN: 41510

American (AMR) AF: 0.476 AC: 7273 AN: 15266

Ashkenazi Jewish (ASJ) AF: 0.339 AC: 1174 AN: 3466

East Asian (EAS) AF: 0.576 AC: 2962 AN: 5142

South Asian (SAS) AF: 0.380 AC: 1830 AN: 4814

European-Finnish (FIN) AF: 0.375 AC: 3950 AN: 10546

Middle Eastern (MID) AF: 0.288 AC: 84 AN: 292

European-Non Finnish (NFE) AF: 0.362 AC: 24568 AN: 67952

Other (OTH) AF: 0.356 AC: 751 AN: 2108

Alfa AF: 0.354 Hom.: 42331

Bravo AF: 0.326

Asia WGS AF: 0.451 AC: 1569 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	5.1
DANN	Benign	0.64
PhyloP100		0.30

Splicing

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

Other links and lift over

dbSNP: rs1925035; hg19: chr1-157909525;