Original source

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

Alleles
CTT/-
Location

Chromosome 1:201361972-201361974 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 5868

This variation has 27 HGVS names - click the plus to show

1:g.201361972_201361974delCTT
ENST00000367318.6:c.628_630delAAG
ENSP00000356287.5:p.Lys210del
ENST00000491504.2:n.1867_1869delAAG
ENST00000458432.3:c.442_444delAAG
ENSP00000387874.3:p.Lys148del
ENST00000460780.2:n.951_953delAAG
ENST00000367317.5:c.610_612delAAG
ENSP00000356286.5:p.Lys204del
ENST00000367315.3:c.637_639delAAG
ENSP00000356284.3:p.Lys213del
ENST00000360372.5:c.529_531delAAG
ENSP00000353535.5:p.Lys177del
ENST00000421663.3:c.442_444delAAG
ENSP00000404134.3:p.Lys148del
ENST00000367322.2:c.619_621delAAG
ENSP00000356291.1:p.Lys207del
ENST00000509001.2:c.628_630delAAG
ENSP00000422031.1:p.Lys210del
ENST00000476888.2:n.113_115delAAG
ENST00000438742.2:c.610_612delAAG
ENSP00000414036.1:p.Lys204del
ENST00000367320.3:c.529_531delAAG
ENSP00000356289.2:p.Lys177del
ENST00000515042.2:n.554_556delAAG
ENST00000236918.8:c.658_660delAAG
ENSP00000236918.8:p.Lys220del

Variation displays