Original source

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

Alleles
TAT/-
Location

Chromosome 11:112088974-112088976 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 11381

This variation has 23 HGVS names - click the plus to show

11:g.112088974_112088976delTAT
ENST00000528182.3:c.277_279delTAT
ENSP00000435475.1:p.Tyr93del
ENST00000525987.3:n.283_285delATT
ENST00000534010.1:c.108_110delTAT
ENSP00000433202.1:p.Tyr37del
ENST00000526592.3:c.277_279delTAT
ENSP00000432005.1:p.Tyr93del
ENST00000614349.2:c.277_279delTAT
ENSP00000480666.1:p.Tyr93del
ENST00000532699.1:c.278_280delATT
ENSP00000456434.1:p.Tyr93del
ENST00000375549.5:c.277_279delTAT
ENSP00000364699.3:p.Tyr93del
ENST00000525291.3:c.160_162delTAT
ENSP00000436669.1:p.Tyr54del
ENST00000528021.3:c.277_279delTAT
ENSP00000432465.1:p.Tyr93del
ENST00000530923.3:c.267_269delTAT
ENSP00000432946.1:p.Tyr90del
ENST00000531744.3:c.278_280delATT
ENSP00000456957.1:p.Tyr93del
ENST00000528048.3:c.169+1001_169+1003delTAT

Variation displays