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 7:94420604 (forward strand)|View in location tab

Co-located variants

COSMIC COSM226177 ; HGMD-PUBLIC CM910090

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 12 HGVS names - Hide

7:g.94420604G>A
ENST00000297268.10:c.2251G>A
ENSP00000297268.6:p.Gly751Ser
ENST00000473573.5:n.588G>A
ENST00000620463.1:c.2245G>A
ENSP00000477719.1:p.Gly749Ser
ENST00000461525.5:n.340G>A
ENST00000497316.5:n.648G>A
ENST00000467931.1:n.271G>A
LRG_2:g.31044G>A
LRG_2t1:c.2251G>A
LRG_2p1:p.Gly751Ser

About this variant

This variant overlaps 11 transcripts and is associated with 2 phenotypes.

Variant displays