Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 7:55249005 (forward strand) | View in location tab

Co-located

with COSMIC COSM291998 (G/C), COSM12989 (G/A), COSM6241 (G/T)

Most severe consequence
Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

Variation displays