Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 7:94424345 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3924262 ; HGMD-PUBLIC CM042017

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 10 HGVS names - Hide

7:g.94424345G>A
ENST00000469732.1:n.358G>A
ENST00000481570.5:n.1875G>A
ENST00000297268.10:c.2575G>A
ENSP00000297268.6:p.Gly859Ser
ENST00000620463.1:c.2569G>A
ENSP00000477719.1:p.Gly857Ser
LRG_2:g.34785G>A
LRG_2t1:c.2575G>A
LRG_2p1:p.Gly859Ser

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays