rs755805

Variant names:

• chr1-190534836-C-T
• rs755805

Variant summary

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

The variant allele was found at a frequency of 0.114 in 151,408 control chromosomes in the GnomAD database, including 1,291 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 0.11 (1291 hom., cov: 32)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.364
• Publications: 3 publications found

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.203 is higher than 0.05.

Variant Effect in Transcripts

 

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Frequencies

GnomAD3 genomes AF: 0.114 AC: 17190 AN: 151288 Hom.: 1275 Cov.: 32

Gnomad AFR AF: 0.0329

Gnomad AMI AF: 0.173

Gnomad AMR AF: 0.208

Gnomad ASJ AF: 0.0812

Gnomad EAS AF: 0.153

Gnomad SAS AF: 0.0639

Gnomad FIN AF: 0.154

Gnomad MID AF: 0.0796

Gnomad NFE AF: 0.137

Gnomad OTH AF: 0.117

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

GnomAD4 genome AF: 0.114 AC: 17224 AN: 151408 Hom.: 1291 Cov.: 32 AF XY: 0.115 AC XY: 8492 AN XY: 73948

African (AFR) AF: 0.0328 AC: 1359 AN: 41468

American (AMR) AF: 0.209 AC: 3162 AN: 15126

Ashkenazi Jewish (ASJ) AF: 0.0812 AC: 281 AN: 3460

East Asian (EAS) AF: 0.153 AC: 786 AN: 5142

South Asian (SAS) AF: 0.0637 AC: 307 AN: 4816

European-Finnish (FIN) AF: 0.154 AC: 1626 AN: 10534

Middle Eastern (MID) AF: 0.0782 AC: 23 AN: 294

European-Non Finnish (NFE) AF: 0.137 AC: 9260 AN: 67554

Other (OTH) AF: 0.125 AC: 262 AN: 2102

Alfa AF: 0.133 Hom.: 2325

Bravo AF: 0.119

Asia WGS AF: 0.137 AC: 476 AN: 3470

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	3.2
DANN	Benign	0.69
PhyloP100		-0.36

Splicing

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

Other links and lift over

dbSNP: rs755805; hg19: chr1-190503966;