Original source

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

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

Chromosome 7:55191831 (forward strand) | View in location tab

Co-located

with COSMIC COSM6213 (T/A), COSM12374 (T/G)

Most severe consequence
Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts.

Variation displays