Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)

Chromosome 7:44188923 (forward strand) | View in location tab


with COSMIC COSM3394777 (C/T)

Most severe consequence
Evidence status


Uniprot VAR_010583

This variation has 6 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 1095 individual genotypes.

Variation displays