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 7:94418508 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM070864

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

7:g.94418508G>A
ENST00000473573.3:n.318G>A
ENST00000297268.8:c.1981G>A
ENSP00000297268.6:p.Gly661Ser
ENST00000620463.1:c.1975G>A
ENSP00000477719.1:p.Gly659Ser
ENST00000461525.3:n.70G>A
ENST00000497316.3:n.378G>A
LRG_2:g.28948G>A
LRG_2t1.1:c.1981G>A
LRG_2p1.1:p.Gly661Ser

Variation displays