This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N
Location

Chromosome 7:55174014 (forward strand) | View in location tab

Co-located

with COSMIC COSM6252 (G/A), COSM6253 (G/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 8 synonyms - click the plus to show

This variation has 33 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts, is associated with 5 phenotypes and is mentioned in 2 citations.

Variation displays