Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 7:94057679 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041284

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

7:g.94057679G>T
ENST00000481570.1:n.4382G>T
ENST00000297268.6:c.3601G>T
ENSP00000297268.6:p.Glu1201Ter
ENST00000464916.1:n.649G>T
LRG_2:g.38807G>T
LRG_2t1.1:c.3601G>T
LRG_2p1.1:p.Glu1201Ter

Variation displays