Original source

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

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

Chromosome 7:55249007 (forward strand) | View in location tab

Co-located

with COSMIC COSM6242 (G/T), COSM13425 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_069503

This variation has 27 HGVS names - click the plus to show

Variation displays