Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

T/C/G|Ancestral: T|Ambiguity code: B

Chromosome 14:73186869 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM003614, CM055498, CM043770

Most severe consequence
Missense variant
Evidence status

Clinical significance

HGVS names

This variant has 30 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and is associated with 3 phenotypes.

Variant displays