Original source

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

Alleles
-/A
Location

Chromosome 5: between 131726531 and 131726532 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 11838

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

5:g.131726531dupA
ENST00000245407.3:c.1202dupA
ENSP00000245407.3:p.Tyr401Ter
ENST00000435065.2:c.1274dupA
ENSP00000402760.2:p.Tyr425Ter
ENST00000475308.1:n.1880dupA
ENST00000461013.1:n.8624dupA
ENST00000447841.1:c.112-1594dupA
ENST00000479605.1:n.305dupA
ENST00000448810.1:c.*54dupA

Variation displays