Original source

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

Alleles
TAT/-
Location

Chromosome 11:111959698-111959700 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 11381

This variation has 22 HGVS names - click the plus to show

11:g.111959698_111959700delTAT
ENST00000528182.1:c.277_279delTAT
ENSP00000435475.1:p.Tyr93del
ENST00000525987.1:n.282_284delTAT
ENST00000534010.1:c.108_110delTAT
ENSP00000433202.1:p.Tyr37del
ENST00000526592.1:c.277_279delTAT
ENSP00000432005.1:p.Tyr93del
HG388_HG400_PATCH:g.111959697_111959699delTAT
ENST00000532699.1:c.277_279delTAT
ENSP00000456434.1:p.Tyr93del
ENST00000375549.3:c.277_279delTAT
ENSP00000364699.3:p.Tyr93del
ENST00000525291.1:c.160_162delTAT
ENSP00000436669.1:p.Tyr54del
ENST00000528021.1:c.277_279delTAT
ENSP00000432465.1:p.Tyr93del
ENST00000531744.1:c.277_279delTAT
ENSP00000456957.1:p.Tyr93del
ENST00000530923.1:c.267_269delTAT
ENSP00000432946.1:p.Tyr90del
ENST00000528048.1:c.169+1001_169+1003delTAT

Variation displays