Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 12:25380275 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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

Variation displays