Original source

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

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

Chromosome 7:94410429 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM001074

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 8 HGVS names - Hide

7:g.94410429G>T
ENST00000620463.1:c.1093G>T
ENSP00000477719.1:p.Gly365Trp
ENST00000297268.10:c.1099G>T
ENSP00000297268.6:p.Gly367Trp
LRG_2:g.20869G>T
LRG_2t1:c.1099G>T
LRG_2p1:p.Gly367Trp

About this variant

This variant overlaps 5 transcripts and is associated with 2 phenotypes.

Variant displays