Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 9:37436699 (forward strand) | View in location tab

Co-located

with COSMIC COSM608894 (C/G) ; HGMD-PUBLIC CM033387

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_012203.1:c.904C>T

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and is associated with 2 phenotypes.

Variant displays