Original source

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

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

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


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

Most severe consequence
Clinical significance

This variation has 2 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 and is associated with 1 phenotype.

Variation displays