Original source

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

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

Chromosome 7:107559657 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960489

Most severe consequence
Clinical significance

Synonyms

LSDB 6382

This variation has 12 HGVS names - click the plus to show

7:g.107559657A>G
ENST00000417551.1:c.1483A>G
ENSP00000390667.1:p.Arg495Gly
ENST00000205402.5:c.1483A>G
ENSP00000205402.3:p.Arg495Gly
ENST00000437604.2:c.1339A>G
ENSP00000387542.2:p.Arg447Gly
ENST00000415325.1:c.*1157A>G
ENST00000537148.1:c.1186A>G
ENSP00000442399.1:p.Arg396Gly
ENST00000440410.1:c.1414A>G
ENSP00000417016.1:p.Arg472Gly

Variation displays