Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.41352871C>ACA507690178TGFB1,TMEM91c.174G>T (p.Arg58=)
c.-30+1669C>A (n.-30+1669C>A)
n.350+1669C>A
19g.41352871C>GCA507690180TGFB1,TMEM91c.174G>C (p.Arg58=)
c.-30+1669C>G (n.-30+1669C>G)
n.350+1669C>G
19g.41352871C>TCA507690179TGFB1,TMEM91c.174G>A (p.Arg58=)
c.-30+1669C>T (n.-30+1669C>T)
n.350+1669C>T
gnomAD v4
19g.41352872C>ACA406005815TGFB1,TMEM91c.173G>T (p.Arg58Leu)
c.-30+1670C>A (n.-30+1670C>A)
n.350+1670C>A
19g.41352872C>GCA406005818TGFB1,TMEM91c.173G>C (p.Arg58Pro)
c.-30+1670C>G (n.-30+1670C>G)
n.350+1670C>G
19g.41352872C>TCA406005821TGFB1,TMEM91c.173G>A (p.Arg58Gln)
c.-30+1670C>T (n.-30+1670C>T)
n.350+1670C>T
gnomAD v4
19g.41352873G>ACA406005825TGFB1,TMEM91c.172C>T (p.Arg58Trp)
c.-30+1671G>A (n.-30+1671G>A)
n.350+1671G>A
gnomAD v4
19g.41352873G>CCA406005827TGFB1,TMEM91c.172C>G (p.Arg58Gly)
c.-30+1671G>C (n.-30+1671G>C)
n.350+1671G>C
19g.41352873G>TCA507690181TGFB1,TMEM91c.172C>A (p.Arg58=)
c.-30+1671G>T (n.-30+1671G>T)
n.350+1671G>T
gnomAD v4
19g.41352874C>ACA507690182TGFB1,TMEM91c.171G>T (p.Leu57=)
c.-30+1672C>A (n.-30+1672C>A)
n.350+1672C>A
dbSNP
19g.41352874C=CA2336426144TGFB1,TMEM91c.171G= (p.Leu57=)
c.-30+1672C= (n.-30+1672C=)
n.350+1672C=
19g.41352874C>GCA507690183TGFB1,TMEM91c.171G>C (p.Leu57=)
c.-30+1672C>G (n.-30+1672C>G)
n.350+1672C>G
19g.41352874C>TCA507690184TGFB1,TMEM91c.171G>A (p.Leu57=)
c.-30+1672C>T (n.-30+1672C>T)
n.350+1672C>T
gnomAD v4
19g.41352875A>CCA406005830TGFB1,TMEM91c.170T>G (p.Leu57Arg)
c.-30+1673A>C (n.-30+1673A>C)
n.350+1673A>C
19g.41352875A>GCA406005833TGFB1,TMEM91c.170T>C (p.Leu57Pro)
c.-30+1673A>G (n.-30+1673A>G)
n.350+1673A>G
19g.41352875A>TCA406005836TGFB1,TMEM91c.170T>A (p.Leu57Gln)
c.-30+1673A>T (n.-30+1673A>T)
n.350+1673A>T
19g.41352876G>ACA507690185TGFB1,TMEM91c.169C>T (p.Leu57=)
c.-30+1674G>A (n.-30+1674G>A)
n.350+1674G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41352876G>CCA406005839TGFB1,TMEM91c.169C>G (p.Leu57Val)
c.-30+1674G>C (n.-30+1674G>C)
n.350+1674G>C
19g.41352876G=CA2336426145TGFB1,TMEM91c.169C= (p.Leu57=)
c.-30+1674G= (n.-30+1674G=)
n.350+1674G=
19g.41352876G>TCA406005843TGFB1,TMEM91c.169C>A (p.Leu57Met)
c.-30+1674G>T (n.-30+1674G>T)
n.350+1674G>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352877C>ACA406005846TGFB1,TMEM91c.168G>T (p.Lys56Asn)
c.-30+1675C>A (n.-30+1675C>A)
n.350+1675C>A
gnomAD v4
19g.41352877C>GCA406005848TGFB1,TMEM91c.168G>C (p.Lys56Asn)
c.-30+1675C>G (n.-30+1675C>G)
n.350+1675C>G
19g.41352877C>TCA507690186TGFB1,TMEM91c.168G>A (p.Lys56=)
c.-30+1675C>T (n.-30+1675C>T)
n.350+1675C>T
gnomAD v4
19g.41352878T>ACA406005851TGFB1,TMEM91c.167A>T (p.Lys56Met)
c.-30+1676T>A (n.-30+1676T>A)
n.350+1676T>A
19g.41352878T>CCA406005854TGFB1,TMEM91c.167A>G (p.Lys56Arg)
c.-30+1676T>C (n.-30+1676T>C)
n.350+1676T>C
19g.41352878T>GCA406005857TGFB1,TMEM91c.167A>C (p.Lys56Thr)
c.-30+1676T>G (n.-30+1676T>G)
n.350+1676T>G
gnomAD v4
19g.41352879T>ACA406005860TGFB1,TMEM91c.166A>T (p.Lys56Ter)
c.-30+1677T>A (n.-30+1677T>A)
n.350+1677T>A
19g.41352879T>CCA406005862TGFB1,TMEM91c.166A>G (p.Lys56Glu)
c.-30+1677T>C (n.-30+1677T>C)
n.350+1677T>C
19g.41352879T>GCA406005865TGFB1,TMEM91c.166A>C (p.Lys56Gln)
c.-30+1677T>G (n.-30+1677T>G)
n.350+1677T>G
19g.41352880G>ACA507690189TGFB1,TMEM91c.165C>T (p.Ser55=)
c.-30+1678G>A (n.-30+1678G>A)
n.350+1678G>A
gnomAD v4
19g.41352880G>CCA507690188TGFB1,TMEM91c.165C>G (p.Ser55=)
c.-30+1678G>C (n.-30+1678G>C)
n.350+1678G>C
gnomAD v4
19g.41352880G>TCA507690187TGFB1,TMEM91c.165C>A (p.Ser55=)
c.-30+1678G>T (n.-30+1678G>T)
n.350+1678G>T
gnomAD v4
19g.41352881G>ACA406005869TGFB1,TMEM91c.164C>T (p.Ser55Phe)
c.-30+1679G>A (n.-30+1679G>A)
n.350+1679G>A
19g.41352881G>CCA406005871TGFB1,TMEM91c.164C>G (p.Ser55Cys)
c.-30+1679G>C (n.-30+1679G>C)
n.350+1679G>C
gnomAD v4
19g.41352881G>TCA406005875TGFB1,TMEM91c.164C>A (p.Ser55Tyr)
c.-30+1679G>T (n.-30+1679G>T)
n.350+1679G>T
gnomAD v4
19g.41352882A=CA2336426146TGFB1,TMEM91c.163T= (p.Ser55=)
c.-30+1680A= (n.-30+1680A=)
n.350+1680A=
19g.41352882A>CCA406005882TGFB1,TMEM91c.163T>G (p.Ser55Ala)
c.-30+1680A>C (n.-30+1680A>C)
n.350+1680A>C
19g.41352882A>GCA308518620TGFB1,TMEM91c.163T>C (p.Ser55Pro)
c.-30+1680A>G (n.-30+1680A>G)
n.350+1680A>G
dbSNP
19g.41352882A>TCA406005879TGFB1,TMEM91c.163T>A (p.Ser55Thr)
c.-30+1680A>T (n.-30+1680A>T)
n.350+1680A>T
19g.41352883C>ACA507690190TGFB1,TMEM91c.162G>T (p.Leu54=)
c.-30+1681C>A (n.-30+1681C>A)
n.350+1681C>A
19g.41352883C=CA2336426147TGFB1,TMEM91c.162G= (p.Leu54=)
c.-30+1681C= (n.-30+1681C=)
n.350+1681C=
19g.41352883C>GCA507690191TGFB1,TMEM91c.162G>C (p.Leu54=)
c.-30+1681C>G (n.-30+1681C>G)
n.350+1681C>G
gnomAD v4
19g.41352883C>TCA507690192TGFB1,TMEM91c.162G>A (p.Leu54=)
c.-30+1681C>T (n.-30+1681C>T)
n.350+1681C>T
dbSNP gnomAD v4
19g.41352884A>CCA406005886TGFB1,TMEM91c.161T>G (p.Leu54Arg)
c.-30+1682A>C (n.-30+1682A>C)
n.350+1682A>C
19g.41352884A>GCA406005888TGFB1,TMEM91c.161T>C (p.Leu54Pro)
c.-30+1682A>G (n.-30+1682A>G)
n.350+1682A>G
gnomAD v4
19g.41352884A>TCA406005891TGFB1,TMEM91c.161T>A (p.Leu54Gln)
c.-30+1682A>T (n.-30+1682A>T)
n.350+1682A>T
19g.41352885G>ACA507690193TGFB1,TMEM91c.160C>T (p.Leu54=)
c.-30+1683G>A (n.-30+1683G>A)
n.350+1683G>A
dbSNP gnomAD v2 gnomAD v4
19g.41352885G>CCA406005895TGFB1,TMEM91c.160C>G (p.Leu54Val)
c.-30+1683G>C (n.-30+1683G>C)
n.350+1683G>C
19g.41352885G=CA2336426148TGFB1,TMEM91c.160C= (p.Leu54=)
c.-30+1683G= (n.-30+1683G=)
n.350+1683G=
19g.41352885G>TCA406005898TGFB1,TMEM91c.160C>A (p.Leu54Met)
c.-30+1683G>T (n.-30+1683G>T)
n.350+1683G>T
gnomAD v4

Number of alleles fetched