Original source

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

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

Chromosome 5:131726525 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM014409

Most severe consequence
Clinical significance

Synonyms

LSDB 11845

This variation has 10 HGVS names - click the plus to show

5:g.131726525G>A
ENST00000245407.3:c.1196G>A
ENSP00000245407.3:p.Arg399Gln
ENST00000435065.2:c.1268G>A
ENSP00000402760.2:p.Arg423Gln
ENST00000475308.1:n.1874G>A
ENST00000461013.1:n.8618G>A
ENST00000447841.1:c.112-1600G>A
ENST00000479605.1:n.299G>A
ENST00000448810.1:c.*48G>A

Variation displays