Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 7:55181312 (forward strand) | View in location tab

Co-located

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

Most severe consequence
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 6 transcripts.

Variation displays