Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 19:14564841 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB TECR_P182L

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

19:g.14564841C>T
ENST00000601461.1:n.629C>T
ENST00000600395.3:n.286C>T
ENST00000599101.3:n.148C>T
ENST00000593637.3:n.716C>T
ENST00000596073.3:c.80C>T
ENSP00000472697.1:p.Pro27Leu
ENST00000601350.3:n.92C>T
ENST00000598333.3:c.*192C>T
ENST00000597607.3:n.585C>T
ENST00000593775.3:n.144C>T
ENST00000594545.3:c.80C>T
ENSP00000469343.1:p.Pro27Leu
ENST00000601187.1:c.115C>T
ENSP00000472957.1:p.Leu39Phe
ENST00000596953.3:n.601C>T
ENST00000598987.3:c.*432C>T
ENST00000215567.7:c.545C>T
ENSP00000215567.4:p.Pro182Leu
ENST00000600083.3:c.80C>T
ENSP00000472114.1:p.Pro27Leu
ENST00000598298.3:c.80C>T
ENSP00000471341.1:p.Pro27Leu

Variation displays