This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 7:55181314 (forward strand) | View in location tab


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

Most severe consequence
Evidence status

Clinical significance


Uniprot VAR_069503

This variation has 36 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts and is associated with 2 phenotypes.

Variation displays