Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.46014277A>TCA225473MAPTc.863A>T (p.Lys288Met)
c.776A>T (p.Lys259Met)
c.950A>T (p.Lys317Met)
n.721A>T
n.176A>T
n.119A>T
c.2126A>T (p.Lys709Met)
c.1835A>T (p.Lys612Met)
c.770A>T (p.Lys257Met)
c.1901A>T (p.Lys634Met)
c.683A>T (p.Lys228Met)
c.1955A>T (p.Lys652Met)
c.857A>T (p.Lys286Met)
n.777-4341A>T
n.6142A>T
c.2213A>T (p.Lys738Met)
c.2120A>T (p.Lys707Met)
c.2039A>T (p.Lys680Met)
c.2015A>T (p.Lys672Met)
c.1922A>T (p.Lys641Met)
c.1148A>T (p.Lys383Met)
c.1061A>T (p.Lys354Met)
c.974A>T (p.Lys325Met)
n.781A>T
ClinVar dbSNP
17g.46014277A=CA2262102718MAPTc.863A= (p.Lys288=)
c.776A= (p.Lys259=)
c.950A= (p.Lys317=)
n.721A=
n.176A=
n.119A=
c.2126A= (p.Lys709=)
c.1835A= (p.Lys612=)
c.770A= (p.Lys257=)
c.1901A= (p.Lys634=)
c.683A= (p.Lys228=)
c.1955A= (p.Lys652=)
c.857A= (p.Lys286=)
n.777-4341A=
n.6142A=
c.2213A= (p.Lys738=)
c.2120A= (p.Lys707=)
c.2039A= (p.Lys680=)
c.2015A= (p.Lys672=)
c.1922A= (p.Lys641=)
c.1148A= (p.Lys383=)
c.1061A= (p.Lys354=)
c.974A= (p.Lys325=)
n.781A=
dbSNP

Number of alleles fetched