Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Co-located

with COSMIC COSM3924262 (G/A) ; HGMD-PUBLIC CM042017

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.94424345G>A
ENST00000469732.1:n.358G>A
ENST00000481570.3:n.1875G>A
ENST00000297268.8: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

Variation displays