Original source

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

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

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

Co-located

with HGMD-PUBLIC CM001074

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.94410429G>T
ENST00000620463.1:c.1093G>T
ENSP00000477719.1:p.Gly365Trp
ENST00000297268.8:c.1099G>T
ENSP00000297268.6:p.Gly367Trp
LRG_2:g.20869G>T
LRG_2t1:c.1099G>T
LRG_2p1:p.Gly367Trp

Variation displays