Original source

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

T/A/G | Ancestral: T | Ambiguity code: D

Chromosome 12:25227341 (forward strand) | View in location tab


with COSMIC COSM1146992 (T/A), COSM1135364 (T/G), COSM554 (T/G), COSM555 (T/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2 individual genotypes and is associated with 2 phenotypes.

Variation displays