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 COSM947 (T/C), COSM948 (T/A) ; 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

Variation displays