Original source

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

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

Chromosome 9:104822520 (forward strand)|View in location tab

Co-located variants

COSMIC COSM301590 ; HGMD-PUBLIC CM990006

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 3 HGVS names - Hide

9:g.104822520T>C
ENST00000374736.7:c.2804A>G
ENSP00000363868.3:p.Asn935Ser

About this variant

This variant overlaps 2 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays