Original source

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

T/A/C | Ancestral: T | Ambiguity code: H

Chromosome 5:150054082 (forward strand) | View in location tab


with COSMIC COSM948 (T/A), COSM947 (T/C) ; HGMD-PUBLIC CM900079

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and has 1 individual genotype.

Variation displays