Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 7:94049916 (forward strand) | View in location tab

Co-located

with COSMIC COSM226177 (G/A) ; HGMD-PUBLIC CM910090

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

7:g.94049916G>A
ENST00000297268.6:c.2251G>A
ENSP00000297268.6:p.Gly751Ser
ENST00000473573.1:n.588G>A
ENST00000497316.1:n.648G>A
ENST00000461525.1:n.340G>A
ENST00000467931.1:n.271G>A
LRG_2:g.31044G>A
LRG_2t1.1:c.2251G>A
LRG_2p1.1:p.Gly751Ser

Variation displays