Original source

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

T/C | Ancestral: T | Ambiguity code: Y

Chromosome 15:63057028 (forward strand) | View in location tab


with COSMIC COSM3502945 (T/G), COSM3502947 (T/G), COSM3502949 (T/G), COSM3502946 (T/G), COSM3502948 (T/G) ; HGMD-PUBLIC CM010475 ; PhenCode FHC0616 (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 44 HGVS names - click the plus to show

About this variant

This variant overlaps 28 transcripts, is associated with 2 phenotypes and is mentioned in 2 citations.

Variation displays