Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
19g.41352886G>ACA9460167TGFB1,TMEM91c.159C>T (p.Ile53=)
c.-30+1684G>A (n.-30+1684G>A)
n.350+1684G>A
 ClinVar dbSNP ExAC gnomAD v4
19g.41352886G>CCA406005900TGFB1,TMEM91c.159C>G (p.Ile53Met)
c.-30+1684G>C (n.-30+1684G>C)
n.350+1684G>C
19g.41352886G=CA2336426149TGFB1,TMEM91c.159C= (p.Ile53=)
c.-30+1684G= (n.-30+1684G=)
n.350+1684G=
19g.41352886G>TCA507690194TGFB1,TMEM91c.159C>A (p.Ile53=)
c.-30+1684G>T (n.-30+1684G>T)
n.350+1684G>T
 gnomAD v4
19g.41352887A=CA2336426150TGFB1,TMEM91c.158T= (p.Ile53=)
c.-30+1685A= (n.-30+1685A=)
n.350+1685A=
19g.41352887A>CCA406005901TGFB1,TMEM91c.158T>G (p.Ile53Ser)
c.-30+1685A>C (n.-30+1685A>C)
n.350+1685A>C
 gnomAD v4
19g.41352887A>GCA9460168TGFB1,TMEM91c.158T>C (p.Ile53Thr)
c.-30+1685A>G (n.-30+1685A>G)
n.350+1685A>G
 ClinVar dbSNP ExAC gnomAD v2
19g.41352887A>TCA406005904TGFB1,TMEM91c.158T>A (p.Ile53Asn)
c.-30+1685A>T (n.-30+1685A>T)
n.350+1685A>T
19g.41352888T>ACA406005908TGFB1,TMEM91c.157A>T (p.Ile53Phe)
c.-30+1686T>A (n.-30+1686T>A)
n.350+1686T>A
19g.41352888T>CCA406005910TGFB1,TMEM91c.157A>G (p.Ile53Val)
c.-30+1686T>C (n.-30+1686T>C)
n.350+1686T>C
19g.41352888T>GCA406005911TGFB1,TMEM91c.157A>C (p.Ile53Leu)
c.-30+1686T>G (n.-30+1686T>G)
n.350+1686T>G
19g.41352889C>ACA406005913TGFB1,TMEM91c.156G>T (p.Gln52His)
c.-30+1687C>A (n.-30+1687C>A)
n.350+1687C>A
 gnomAD v4
19g.41352889C>GCA406005912TGFB1,TMEM91c.156G>C (p.Gln52His)
c.-30+1687C>G (n.-30+1687C>G)
n.350+1687C>G
19g.41352889C>TCA507690195TGFB1,TMEM91c.156G>A (p.Gln52=)
c.-30+1687C>T (n.-30+1687C>T)
n.350+1687C>T
19g.41352890T>ACA406005914TGFB1,TMEM91c.155A>T (p.Gln52Leu)
c.-30+1688T>A (n.-30+1688T>A)
n.350+1688T>A
19g.41352890T>CCA406005921TGFB1,TMEM91c.155A>G (p.Gln52Arg)
c.-30+1688T>C (n.-30+1688T>C)
n.350+1688T>C
 gnomAD v4
19g.41352890T>GCA406005918TGFB1,TMEM91c.155A>C (p.Gln52Pro)
c.-30+1688T>G (n.-30+1688T>G)
n.350+1688T>G
19g.41352891G>ACA406005923TGFB1,TMEM91c.154C>T (p.Gln52Ter)
c.-30+1689G>A (n.-30+1689G>A)
n.350+1689G>A
 dbSNP gnomAD v2
19g.41352891G>CCA406005926TGFB1,TMEM91c.154C>G (p.Gln52Glu)
c.-30+1689G>C (n.-30+1689G>C)
n.350+1689G>C
19g.41352891G=CA2336426151TGFB1,TMEM91c.154C= (p.Gln52=)
c.-30+1689G= (n.-30+1689G=)
n.350+1689G=
19g.41352891G>TCA406005928TGFB1,TMEM91c.154C>A (p.Gln52Lys)
c.-30+1689G>T (n.-30+1689G>T)
n.350+1689G>T
19g.41352892G>ACA507690196TGFB1,TMEM91c.153C>T (p.Gly51=)
c.-30+1690G>A (n.-30+1690G>A)
n.350+1690G>A
 dbSNP gnomAD v3 gnomAD v4
19g.41352892G>CCA507690197TGFB1,TMEM91c.153C>G (p.Gly51=)
c.-30+1690G>C (n.-30+1690G>C)
n.350+1690G>C
19g.41352892G=CA2336426152TGFB1,TMEM91c.153C= (p.Gly51=)
c.-30+1690G= (n.-30+1690G=)
n.350+1690G=
19g.41352892G>TCA507690198TGFB1,TMEM91c.153C>A (p.Gly51=)
c.-30+1690G>T (n.-30+1690G>T)
n.350+1690G>T
 gnomAD v4
19g.41352893C>ACA406005929TGFB1,TMEM91c.152G>T (p.Gly51Val)
c.-30+1691C>A (n.-30+1691C>A)
n.350+1691C>A
 gnomAD v4
19g.41352893C>GCA406005930TGFB1,TMEM91c.152G>C (p.Gly51Ala)
c.-30+1691C>G (n.-30+1691C>G)
n.350+1691C>G
19g.41352893C>TCA406005931TGFB1,TMEM91c.152G>A (p.Gly51Asp)
c.-30+1691C>T (n.-30+1691C>T)
n.350+1691C>T
 gnomAD v4
19g.41352894C>ACA406005934TGFB1,TMEM91c.151G>T (p.Gly51Cys)
c.-30+1692C>A (n.-30+1692C>A)
n.350+1692C>A
19g.41352894C>GCA406005939TGFB1,TMEM91c.151G>C (p.Gly51Arg)
c.-30+1692C>G (n.-30+1692C>G)
n.350+1692C>G
 ClinVar
19g.41352894C>TCA406005941TGFB1,TMEM91c.151G>A (p.Gly51Ser)
c.-30+1692C>T (n.-30+1692C>T)
n.350+1692C>T
19g.41352895G>ACA507690199TGFB1,TMEM91c.150C>T (p.Arg50=)
c.-30+1693G>A (n.-30+1693G>A)
n.350+1693G>A
 dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched