Original source

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

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

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

Co-located

with COSMIC COSM301590 (T/C) ; HGMD-PUBLIC CM990006

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

This variant has 3 HGVS names - click the plus to show

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