Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
19g.41352895G>CCA507690200TGFB1,TMEM91c.150C>G (p.Arg50=)
c.-30+1693G>C (n.-30+1693G>C)
n.350+1693G>C
19g.41352895G=CA2336426153TGFB1,TMEM91c.150C= (p.Arg50=)
c.-30+1693G= (n.-30+1693G=)
n.350+1693G=
19g.41352895G>TCA507690201TGFB1,TMEM91c.150C>A (p.Arg50=)
c.-30+1693G>T (n.-30+1693G>T)
n.350+1693G>T
 gnomAD v4
19g.41352896C>ACA406005945TGFB1,TMEM91c.149G>T (p.Arg50Leu)
c.-30+1694C>A (n.-30+1694C>A)
n.350+1694C>A
 dbSNP gnomAD v3 gnomAD v4
19g.41352896C>GCA406005949TGFB1,TMEM91c.149G>C (p.Arg50Pro)
c.-30+1694C>G (n.-30+1694C>G)
n.350+1694C>G
 gnomAD v4
19g.41352896C>TCA406005953TGFB1,TMEM91c.149G>A (p.Arg50His)
c.-30+1694C>T (n.-30+1694C>T)
n.350+1694C>T
 gnomAD v4
19g.41352897G>ACA406005957TGFB1,TMEM91c.148C>T (p.Arg50Cys)
c.-30+1695G>A (n.-30+1695G>A)
n.350+1695G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41352897G>CCA406005962TGFB1,TMEM91c.148C>G (p.Arg50Gly)
c.-30+1695G>C (n.-30+1695G>C)
n.350+1695G>C
19g.41352897G=CA2336426154TGFB1,TMEM91c.148C= (p.Arg50=)
c.-30+1695G= (n.-30+1695G=)
n.350+1695G=
19g.41352897G>TCA406005960TGFB1,TMEM91c.148C>A (p.Arg50Ser)
c.-30+1695G>T (n.-30+1695G>T)
n.350+1695G>T
 gnomAD v4
19g.41352898G>ACA507690202TGFB1,TMEM91c.147C>T (p.Ile49=)
c.-30+1696G>A (n.-30+1696G>A)
n.350+1696G>A
19g.41352898G>CCA406005965TGFB1,TMEM91c.147C>G (p.Ile49Met)
c.-30+1696G>C (n.-30+1696G>C)
n.350+1696G>C
19g.41352898G>TCA507690203TGFB1,TMEM91c.147C>A (p.Ile49=)
c.-30+1696G>T (n.-30+1696G>T)
n.350+1696G>T
 gnomAD v4
19g.41352899A=CA2336426155TGFB1,TMEM91c.146T= (p.Ile49=)
c.-30+1697A= (n.-30+1697A=)
n.350+1697A=
19g.41352899A>CCA406005970TGFB1,TMEM91c.146T>G (p.Ile49Ser)
c.-30+1697A>C (n.-30+1697A>C)
n.350+1697A>C
 ClinVar dbSNP gnomAD v4
19g.41352899A>GCA406005973TGFB1,TMEM91c.146T>C (p.Ile49Thr)
c.-30+1697A>G (n.-30+1697A>G)
n.350+1697A>G
 gnomAD v4
19g.41352899A>TCA406005977TGFB1,TMEM91c.146T>A (p.Ile49Asn)
c.-30+1697A>T (n.-30+1697A>T)
n.350+1697A>T
19g.41352900T>ACA406005981TGFB1,TMEM91c.145A>T (p.Ile49Phe)
c.-30+1698T>A (n.-30+1698T>A)
n.350+1698T>A
 gnomAD v4
19g.41352900T>CCA406005983TGFB1,TMEM91c.145A>G (p.Ile49Val)
c.-30+1698T>C (n.-30+1698T>C)
n.350+1698T>C
 gnomAD v4
19g.41352900T>GCA406005987TGFB1,TMEM91c.145A>C (p.Ile49Leu)
c.-30+1698T>G (n.-30+1698T>G)
n.350+1698T>G
19g.41352901G>ACA507690206TGFB1,TMEM91c.144C>T (p.Ala48=)
c.-30+1699G>A (n.-30+1699G>A)
n.350+1699G>A
 gnomAD v4
19g.41352901G>CCA507690205TGFB1,TMEM91c.144C>G (p.Ala48=)
c.-30+1699G>C (n.-30+1699G>C)
n.350+1699G>C
 gnomAD v4
19g.41352901G>TCA507690204TGFB1,TMEM91c.144C>A (p.Ala48=)
c.-30+1699G>T (n.-30+1699G>T)
n.350+1699G>T
19g.41352902G>ACA406005991TGFB1,TMEM91c.143C>T (p.Ala48Val)
c.-30+1700G>A (n.-30+1700G>A)
n.350+1700G>A
 gnomAD v4
19g.41352902G>CCA9460169TGFB1,TMEM91c.143C>G (p.Ala48Gly)
c.-30+1700G>C (n.-30+1700G>C)
n.350+1700G>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352902G=CA2336426156TGFB1,TMEM91c.143C= (p.Ala48=)
c.-30+1700G= (n.-30+1700G=)
n.350+1700G=
19g.41352902G>TCA406005996TGFB1,TMEM91c.143C>A (p.Ala48Asp)
c.-30+1700G>T (n.-30+1700G>T)
n.350+1700G>T
 gnomAD v4
19g.41352903C>ACA406006002TGFB1,TMEM91c.142G>T (p.Ala48Ser)
c.-30+1701C>A (n.-30+1701C>A)
n.350+1701C>A
 gnomAD v4
19g.41352903C>GCA406006006TGFB1,TMEM91c.142G>C (p.Ala48Pro)
c.-30+1701C>G (n.-30+1701C>G)
n.350+1701C>G
19g.41352903C>TCA406006000TGFB1,TMEM91c.142G>A (p.Ala48Thr)
c.-30+1701C>T (n.-30+1701C>T)
n.350+1701C>T
 gnomAD v4
19g.41352904C>ACA406006009TGFB1,TMEM91c.141G>T (p.Glu47Asp)
c.-30+1702C>A (n.-30+1702C>A)
n.350+1702C>A
19g.41352904C>GCA406006013TGFB1,TMEM91c.141G>C (p.Glu47Asp)
c.-30+1702C>G (n.-30+1702C>G)
n.350+1702C>G
 gnomAD v4
19g.41352904C>TCA507690207TGFB1,TMEM91c.141G>A (p.Glu47=)
c.-30+1702C>T (n.-30+1702C>T)
n.350+1702C>T
19g.41352905T>ACA406006018TGFB1,TMEM91c.140A>T (p.Glu47Val)
c.-30+1703T>A (n.-30+1703T>A)
n.350+1703T>A
 gnomAD v4
19g.41352905T>CCA308518638TGFB1,TMEM91c.140A>G (p.Glu47Gly)
c.-30+1703T>C (n.-30+1703T>C)
n.350+1703T>C
 dbSNP
19g.41352905T>GCA406006023TGFB1,TMEM91c.140A>C (p.Glu47Ala)
c.-30+1703T>G (n.-30+1703T>G)
n.350+1703T>G
19g.41352905T=CA2336426157TGFB1,TMEM91c.140A= (p.Glu47=)
c.-30+1703T= (n.-30+1703T=)
n.350+1703T=
19g.41352906C>ACA406006024TGFB1,TMEM91c.139G>T (p.Glu47Ter)
c.-30+1704C>A (n.-30+1704C>A)
n.350+1704C>A
 gnomAD v4
19g.41352906C=CA2336426158TGFB1,TMEM91c.139G= (p.Glu47=)
c.-30+1704C= (n.-30+1704C=)
n.350+1704C=
19g.41352906C>GCA406006027TGFB1,TMEM91c.139G>C (p.Glu47Gln)
c.-30+1704C>G (n.-30+1704C>G)
n.350+1704C>G
19g.41352906C>TCA406006030TGFB1,TMEM91c.139G>A (p.Glu47Lys)
c.-30+1704C>T (n.-30+1704C>T)
n.350+1704C>T
 dbSNP gnomAD v4
19g.41352907G>ACA507690209TGFB1,TMEM91c.138C>T (p.Ile46=)
c.-30+1705G>A (n.-30+1705G>A)
n.350+1705G>A
 gnomAD v4
19g.41352907G>CCA406006031TGFB1,TMEM91c.138C>G (p.Ile46Met)
c.-30+1705G>C (n.-30+1705G>C)
n.350+1705G>C
19g.41352907G>TCA507690210TGFB1,TMEM91c.138C>A (p.Ile46=)
c.-30+1705G>T (n.-30+1705G>T)
n.350+1705G>T
 gnomAD v4
19g.41352908A>CCA406006032TGFB1,TMEM91c.137T>G (p.Ile46Ser)
c.-30+1706A>C (n.-30+1706A>C)
n.350+1706A>C
19g.41352908A>GCA406006033TGFB1,TMEM91c.137T>C (p.Ile46Thr)
c.-30+1706A>G (n.-30+1706A>G)
n.350+1706A>G
19g.41352908A>TCA406006035TGFB1,TMEM91c.137T>A (p.Ile46Asn)
c.-30+1706A>T (n.-30+1706A>T)
n.350+1706A>T
19g.41352909T>ACA406006047TGFB1,TMEM91c.136A>T (p.Ile46Phe)
c.-30+1707T>A (n.-30+1707T>A)
n.350+1707T>A
19g.41352909T>CCA406006049TGFB1,TMEM91c.136A>G (p.Ile46Val)
c.-30+1707T>C (n.-30+1707T>C)
n.350+1707T>C
19g.41352909T>GCA406006046TGFB1,TMEM91c.136A>C (p.Ile46Leu)
c.-30+1707T>G (n.-30+1707T>G)
n.350+1707T>G
19g.41352910G>ACA507690212TGFB1,TMEM91c.135C>T (p.Arg45=)
c.-30+1708G>A (n.-30+1708G>A)
n.350+1708G>A
 gnomAD v4
19g.41352910G>CCA507690213TGFB1,TMEM91c.135C>G (p.Arg45=)
c.-30+1708G>C (n.-30+1708G>C)
n.350+1708G>C
19g.41352910G>TCA507690214TGFB1,TMEM91c.135C>A (p.Arg45=)
c.-30+1708G>T (n.-30+1708G>T)
n.350+1708G>T
 gnomAD v4
19g.41352911C>ACA406006052TGFB1,TMEM91c.134G>T (p.Arg45Leu)
c.-30+1709C>A (n.-30+1709C>A)
n.350+1709C>A
 gnomAD v4
19g.41352911C=CA2336426159TGFB1,TMEM91c.134G= (p.Arg45=)
c.-30+1709C= (n.-30+1709C=)
n.350+1709C=
19g.41352911C>GCA406006055TGFB1,TMEM91c.134G>C (p.Arg45Pro)
c.-30+1709C>G (n.-30+1709C>G)
n.350+1709C>G
19g.41352911C>TCA406006057TGFB1,TMEM91c.134G>A (p.Arg45His)
c.-30+1709C>T (n.-30+1709C>T)
n.350+1709C>T
 dbSNP gnomAD v2 gnomAD v4
19g.41352912G>ACA406006064TGFB1,TMEM91c.133C>T (p.Arg45Cys)
c.-30+1710G>A (n.-30+1710G>A)
n.350+1710G>A
 ClinVar dbSNP gnomAD v4
19g.41352912G>CCA406006066TGFB1,TMEM91c.133C>G (p.Arg45Gly)
c.-30+1710G>C (n.-30+1710G>C)
n.350+1710G>C
19g.41352912G=CA2336426160TGFB1,TMEM91c.133C= (p.Arg45=)
c.-30+1710G= (n.-30+1710G=)
n.350+1710G=
19g.41352912G>TCA406006070TGFB1,TMEM91c.133C>A (p.Arg45Ser)
c.-30+1710G>T (n.-30+1710G>T)
n.350+1710G>T
 gnomAD v4
19g.41352913C>ACA406006074TGFB1,TMEM91c.132G>T (p.Lys44Asn)
c.-30+1711C>A (n.-30+1711C>A)
n.350+1711C>A
 gnomAD v4
19g.41352913C>GCA406006072TGFB1,TMEM91c.132G>C (p.Lys44Asn)
c.-30+1711C>G (n.-30+1711C>G)
n.350+1711C>G
19g.41352913C>TCA507690217TGFB1,TMEM91c.132G>A (p.Lys44=)
c.-30+1711C>T (n.-30+1711C>T)
n.350+1711C>T
 gnomAD v4
19g.41352914T>ACA406006077TGFB1,TMEM91c.131A>T (p.Lys44Met)
c.-30+1712T>A (n.-30+1712T>A)
n.350+1712T>A
19g.41352914T>CCA406006080TGFB1,TMEM91c.131A>G (p.Lys44Arg)
c.-30+1712T>C (n.-30+1712T>C)
n.350+1712T>C
19g.41352914T>GCA406006081TGFB1,TMEM91c.131A>C (p.Lys44Thr)
c.-30+1712T>G (n.-30+1712T>G)
n.350+1712T>G
19g.41352915T>ACA406006084TGFB1,TMEM91c.130A>T (p.Lys44Ter)
c.-30+1713T>A (n.-30+1713T>A)
n.350+1713T>A
19g.41352915T>CCA406006086TGFB1,TMEM91c.130A>G (p.Lys44Glu)
c.-30+1713T>C (n.-30+1713T>C)
n.350+1713T>C
 gnomAD v4
19g.41352915T>GCA9460170TGFB1,TMEM91c.130A>C (p.Lys44Gln)
c.-30+1713T>G (n.-30+1713T>G)
n.350+1713T>G
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41352915T=CA2336426161TGFB1,TMEM91c.130A= (p.Lys44=)
c.-30+1713T= (n.-30+1713T=)
n.350+1713T=
19g.41352916C>ACA507690221TGFB1,TMEM91c.129G>T (p.Arg43=)
c.-30+1714C>A (n.-30+1714C>A)
n.350+1714C>A
 gnomAD v4
19g.41352916C=CA2336426162TGFB1,TMEM91c.129G= (p.Arg43=)
c.-30+1714C= (n.-30+1714C=)
n.350+1714C=
19g.41352916C>GCA507690222TGFB1,TMEM91c.129G>C (p.Arg43=)
c.-30+1714C>G (n.-30+1714C>G)
n.350+1714C>G
 gnomAD v4
19g.41352916C>TCA507690223TGFB1,TMEM91c.129G>A (p.Arg43=)
c.-30+1714C>T (n.-30+1714C>T)
n.350+1714C>T
 ClinVar dbSNP gnomAD v4
19g.41352917C>ACA406006090TGFB1,TMEM91c.128G>T (p.Arg43Leu)
c.-30+1715C>A (n.-30+1715C>A)
n.350+1715C>A
 gnomAD v4
19g.41352917C=CA2336426163TGFB1,TMEM91c.128G= (p.Arg43=)
c.-30+1715C= (n.-30+1715C=)
n.350+1715C=
19g.41352917C>GCA406006094TGFB1,TMEM91c.128G>C (p.Arg43Pro)
c.-30+1715C>G (n.-30+1715C>G)
n.350+1715C>G
19g.41352917C>TCA406006092TGFB1,TMEM91c.128G>A (p.Arg43Gln)
c.-30+1715C>T (n.-30+1715C>T)
n.350+1715C>T
 dbSNP gnomAD v2 gnomAD v4 COSMIC
19g.41352918G>ACA406006099TGFB1,TMEM91c.127C>T (p.Arg43Trp)
c.-30+1716G>A (n.-30+1716G>A)
n.350+1716G>A
 gnomAD v4
19g.41352918G>CCA406006102TGFB1,TMEM91c.127C>G (p.Arg43Gly)
c.-30+1716G>C (n.-30+1716G>C)
n.350+1716G>C
19g.41352918G>TCA507690224TGFB1,TMEM91c.127C>A (p.Arg43=)
c.-30+1716G>T (n.-30+1716G>T)
n.350+1716G>T
 gnomAD v4
19g.41352919C>ACA406006105TGFB1,TMEM91c.126G>T (p.Lys42Asn)
c.-30+1717C>A (n.-30+1717C>A)
n.350+1717C>A
 gnomAD v4
19g.41352919C>GCA406006109TGFB1,TMEM91c.126G>C (p.Lys42Asn)
c.-30+1717C>G (n.-30+1717C>G)
n.350+1717C>G
19g.41352919C>TCA507690225TGFB1,TMEM91c.126G>A (p.Lys42=)
c.-30+1717C>T (n.-30+1717C>T)
n.350+1717C>T
 gnomAD v4
19g.41352920T>ACA406006113TGFB1,TMEM91c.125A>T (p.Lys42Met)
c.-30+1718T>A (n.-30+1718T>A)
n.350+1718T>A
 gnomAD v4
19g.41352920T>CCA406006115TGFB1,TMEM91c.125A>G (p.Lys42Arg)
c.-30+1718T>C (n.-30+1718T>C)
n.350+1718T>C
 gnomAD v4
19g.41352920T>GCA406006117TGFB1,TMEM91c.125A>C (p.Lys42Thr)
c.-30+1718T>G (n.-30+1718T>G)
n.350+1718T>G
19g.41352921T>ACA406006120TGFB1,TMEM91c.124A>T (p.Lys42Ter)
c.-30+1719T>A (n.-30+1719T>A)
n.350+1719T>A
19g.41352921T>CCA406006122TGFB1,TMEM91c.124A>G (p.Lys42Glu)
c.-30+1719T>C (n.-30+1719T>C)
n.350+1719T>C
19g.41352921T>GCA406006126TGFB1,TMEM91c.124A>C (p.Lys42Gln)
c.-30+1719T>G (n.-30+1719T>G)
n.350+1719T>G
19g.41352922C>ACA507690229TGFB1,TMEM91c.123G>T (p.Val41=)
c.-30+1720C>A (n.-30+1720C>A)
n.350+1720C>A
 gnomAD v4
19g.41352922C>GCA507690231TGFB1,TMEM91c.123G>C (p.Val41=)
c.-30+1720C>G (n.-30+1720C>G)
n.350+1720C>G
19g.41352922C>TCA507690230TGFB1,TMEM91c.123G>A (p.Val41=)
c.-30+1720C>T (n.-30+1720C>T)
n.350+1720C>T
 gnomAD v4
19g.41352923A=CA2336426164TGFB1,TMEM91c.122T= (p.Val41=)
c.-30+1721A= (n.-30+1721A=)
n.350+1721A=
19g.41352923A>CCA406006131TGFB1,TMEM91c.122T>G (p.Val41Gly)
c.-30+1721A>C (n.-30+1721A>C)
n.350+1721A>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352923A>GCA308518648TGFB1,TMEM91c.122T>C (p.Val41Ala)
c.-30+1721A>G (n.-30+1721A>G)
n.350+1721A>G
 dbSNP gnomAD v4
19g.41352923A>TCA406006137TGFB1,TMEM91c.122T>A (p.Val41Glu)
c.-30+1721A>T (n.-30+1721A>T)
n.350+1721A>T
19g.41352924C>ACA406006144TGFB1,TMEM91c.121G>T (p.Val41Leu)
c.-30+1722C>A (n.-30+1722C>A)
n.350+1722C>A
 dbSNP gnomAD v2 gnomAD v4
19g.41352924C=CA2336426165TGFB1,TMEM91c.121G= (p.Val41=)
c.-30+1722C= (n.-30+1722C=)
n.350+1722C=
19g.41352924C>GCA406006147TGFB1,TMEM91c.121G>C (p.Val41Leu)
c.-30+1722C>G (n.-30+1722C>G)
n.350+1722C>G
 gnomAD v4
19g.41352924C>TCA406006149TGFB1,TMEM91c.121G>A (p.Val41Met)
c.-30+1722C>T (n.-30+1722C>T)
n.350+1722C>T
 dbSNP gnomAD v4
19g.41352925C>ACA507690233TGFB1,TMEM91c.120G>T (p.Leu40=)
c.-30+1723C>A (n.-30+1723C>A)
n.350+1723C>A
 gnomAD v4
19g.41352925C=CA2336426166TGFB1,TMEM91c.120G= (p.Leu40=)
c.-30+1723C= (n.-30+1723C=)
n.350+1723C=
19g.41352925C>GCA507690234TGFB1,TMEM91c.120G>C (p.Leu40=)
c.-30+1723C>G (n.-30+1723C>G)
n.350+1723C>G
 dbSNP gnomAD v2 gnomAD v4
19g.41352925C>TCA507690235TGFB1,TMEM91c.120G>A (p.Leu40=)
c.-30+1723C>T (n.-30+1723C>T)
n.350+1723C>T
 dbSNP gnomAD v2 gnomAD v4
19g.41352926A>CCA406006153TGFB1,TMEM91c.119T>G (p.Leu40Arg)
c.-30+1724A>C (n.-30+1724A>C)
n.350+1724A>C
 gnomAD v4
19g.41352926A>GCA406006158TGFB1,TMEM91c.119T>C (p.Leu40Pro)
c.-30+1724A>G (n.-30+1724A>G)
n.350+1724A>G
 gnomAD v4
19g.41352926A>TCA406006156TGFB1,TMEM91c.119T>A (p.Leu40Gln)
c.-30+1724A>T (n.-30+1724A>T)
n.350+1724A>T
 gnomAD v4
19g.41352927G>ACA507690236TGFB1,TMEM91c.118C>T (p.Leu40=)
c.-30+1725G>A (n.-30+1725G>A)
n.350+1725G>A
 gnomAD v4
19g.41352927G>CCA406006160TGFB1,TMEM91c.118C>G (p.Leu40Val)
c.-30+1725G>C (n.-30+1725G>C)
n.350+1725G>C
 gnomAD v4
19g.41352927G>TCA406006163TGFB1,TMEM91c.118C>A (p.Leu40Met)
c.-30+1725G>T (n.-30+1725G>T)
n.350+1725G>T
 gnomAD v4
19g.41352928C>ACA406006165TGFB1,TMEM91c.117G>T (p.Glu39Asp)
c.-30+1726C>A (n.-30+1726C>A)
n.350+1726C>A
 gnomAD v4
19g.41352928C=CA2336426167TGFB1,TMEM91c.117G= (p.Glu39=)
c.-30+1726C= (n.-30+1726C=)
n.350+1726C=
19g.41352928C>GCA406006167TGFB1,TMEM91c.117G>C (p.Glu39Asp)
c.-30+1726C>G (n.-30+1726C>G)
n.350+1726C>G
19g.41352928C>TCA507690240TGFB1,TMEM91c.117G>A (p.Glu39=)
c.-30+1726C>T (n.-30+1726C>T)
n.350+1726C>T
 dbSNP gnomAD v2 gnomAD v4
19g.41352929T>ACA406006170TGFB1,TMEM91c.116A>T (p.Glu39Val)
c.-30+1727T>A (n.-30+1727T>A)
n.350+1727T>A
19g.41352929T>CCA406006171TGFB1,TMEM91c.116A>G (p.Glu39Gly)
c.-30+1727T>C (n.-30+1727T>C)
n.350+1727T>C
 gnomAD v4
19g.41352929T>GCA406006172TGFB1,TMEM91c.116A>C (p.Glu39Ala)
c.-30+1727T>G (n.-30+1727T>G)
n.350+1727T>G
 ClinVar
19g.41352930C>ACA406006174TGFB1,TMEM91c.115G>T (p.Glu39Ter)
c.-30+1728C>A (n.-30+1728C>A)
n.350+1728C>A
 gnomAD v4
19g.41352930C>GCA406006176TGFB1,TMEM91c.115G>C (p.Glu39Gln)
c.-30+1728C>G (n.-30+1728C>G)
n.350+1728C>G
19g.41352930C>TCA406006178TGFB1,TMEM91c.115G>A (p.Glu39Lys)
c.-30+1728C>T (n.-30+1728C>T)
n.350+1728C>T
 gnomAD v4
19g.41352931C>ACA406006180TGFB1,TMEM91c.114G>T (p.Met38Ile)
c.-30+1729C>A (n.-30+1729C>A)
n.350+1729C>A
19g.41352931C=CA2336426168TGFB1,TMEM91c.114G= (p.Met38=)
c.-30+1729C= (n.-30+1729C=)
n.350+1729C=
19g.41352931C>GCA406006181TGFB1,TMEM91c.114G>C (p.Met38Ile)
c.-30+1729C>G (n.-30+1729C>G)
n.350+1729C>G
19g.41352931C>TCA406006179TGFB1,TMEM91c.114G>A (p.Met38Ile)
c.-30+1729C>T (n.-30+1729C>T)
n.350+1729C>T
 dbSNP gnomAD v2 gnomAD v4
19g.41352932A=CA2336426169TGFB1,TMEM91c.113T= (p.Met38=)
c.-30+1730A= (n.-30+1730A=)
n.350+1730A=
19g.41352932A>CCA406006183TGFB1,TMEM91c.113T>G (p.Met38Arg)
c.-30+1730A>C (n.-30+1730A>C)
n.350+1730A>C
 gnomAD v4
19g.41352932A>GCA308518654TGFB1,TMEM91c.113T>C (p.Met38Thr)
c.-30+1730A>G (n.-30+1730A>G)
n.350+1730A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352932A>TCA406006185TGFB1,TMEM91c.113T>A (p.Met38Lys)
c.-30+1730A>T (n.-30+1730A>T)
n.350+1730A>T
 gnomAD v4
19g.41352933T>ACA308518666TGFB1,TMEM91c.112A>T (p.Met38Leu)
c.-30+1731T>A (n.-30+1731T>A)
n.350+1731T>A
 dbSNP gnomAD v4
19g.41352933T>CCA9460171TGFB1,TMEM91c.112A>G (p.Met38Val)
c.-30+1731T>C (n.-30+1731T>C)
n.350+1731T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41352933T>GCA406006186TGFB1,TMEM91c.112A>C (p.Met38Leu)
c.-30+1731T>G (n.-30+1731T>G)
n.350+1731T>G
 gnomAD v4
19g.41352933T=CA2336426170TGFB1,TMEM91c.112A= (p.Met38=)
c.-30+1731T= (n.-30+1731T=)
n.350+1731T=
19g.41352934G>ACA507690244TGFB1,TMEM91c.111C>T (p.Asp37=)
c.-30+1732G>A (n.-30+1732G>A)
n.350+1732G>A
 gnomAD v4
19g.41352934G>CCA406006187TGFB1,TMEM91c.111C>G (p.Asp37Glu)
c.-30+1732G>C (n.-30+1732G>C)
n.350+1732G>C
19g.41352934G>TCA406006188TGFB1,TMEM91c.111C>A (p.Asp37Glu)
c.-30+1732G>T (n.-30+1732G>T)
n.350+1732G>T
 gnomAD v4
19g.41352935T>ACA406006189TGFB1,TMEM91c.110A>T (p.Asp37Val)
c.-30+1733T>A (n.-30+1733T>A)
n.350+1733T>A
19g.41352935T>CCA406006190TGFB1,TMEM91c.110A>G (p.Asp37Gly)
c.-30+1733T>C (n.-30+1733T>C)
n.350+1733T>C
 gnomAD v4
19g.41352935T>GCA406006191TGFB1,TMEM91c.110A>C (p.Asp37Ala)
c.-30+1733T>G (n.-30+1733T>G)
n.350+1733T>G
19g.41352936C>ACA406006193TGFB1,TMEM91c.109G>T (p.Asp37Tyr)
c.-30+1734C>A (n.-30+1734C>A)
n.350+1734C>A
 dbSNP gnomAD v3 gnomAD v4
19g.41352936C=CA2336426171TGFB1,TMEM91c.109G= (p.Asp37=)
c.-30+1734C= (n.-30+1734C=)
n.350+1734C=
19g.41352936C>GCA406006194TGFB1,TMEM91c.109G>C (p.Asp37His)
c.-30+1734C>G (n.-30+1734C>G)
n.350+1734C>G
 dbSNP gnomAD v2 gnomAD v4
19g.41352936C>TCA406006195TGFB1,TMEM91c.109G>A (p.Asp37Asn)
c.-30+1734C>T (n.-30+1734C>T)
n.350+1734C>T
 gnomAD v4
19g.41352937G>ACA507690247TGFB1,TMEM91c.108C>T (p.Ile36=)
c.-30+1735G>A (n.-30+1735G>A)
n.350+1735G>A
 dbSNP gnomAD v4
19g.41352937G>CCA9460172TGFB1,TMEM91c.108C>G (p.Ile36Met)
c.-30+1735G>C (n.-30+1735G>C)
n.350+1735G>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352937G=CA2336426172TGFB1,TMEM91c.108C= (p.Ile36=)
c.-30+1735G= (n.-30+1735G=)
n.350+1735G=
19g.41352937G>TCA507690248TGFB1,TMEM91c.108C>A (p.Ile36=)
c.-30+1735G>T (n.-30+1735G>T)
n.350+1735G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41352938A>CCA406006196TGFB1,TMEM91c.107T>G (p.Ile36Ser)
c.-30+1736A>C (n.-30+1736A>C)
n.350+1736A>C
19g.41352938A>GCA406006197TGFB1,TMEM91c.107T>C (p.Ile36Thr)
c.-30+1736A>G (n.-30+1736A>G)
n.350+1736A>G
 gnomAD v4
19g.41352938A>TCA406006199TGFB1,TMEM91c.107T>A (p.Ile36Asn)
c.-30+1736A>T (n.-30+1736A>T)
n.350+1736A>T
 gnomAD v4
19g.41352939T>ACA406006201TGFB1,TMEM91c.106A>T (p.Ile36Phe)
c.-30+1737T>A (n.-30+1737T>A)
n.350+1737T>A
19g.41352939T>CCA406006203TGFB1,TMEM91c.106A>G (p.Ile36Val)
c.-30+1737T>C (n.-30+1737T>C)
n.350+1737T>C
19g.41352939T>GCA406006204TGFB1,TMEM91c.106A>C (p.Ile36Leu)
c.-30+1737T>G (n.-30+1737T>G)
n.350+1737T>G
19g.41352940A>CCA507690251TGFB1,TMEM91c.105T>G (p.Thr35=)
c.-30+1738A>C (n.-30+1738A>C)
n.350+1738A>C
19g.41352940A>GCA507690252TGFB1,TMEM91c.105T>C (p.Thr35=)
c.-30+1738A>G (n.-30+1738A>G)
n.350+1738A>G
 gnomAD v4
19g.41352940A>TCA507690253TGFB1,TMEM91c.105T>A (p.Thr35=)
c.-30+1738A>T (n.-30+1738A>T)
n.350+1738A>T
19g.41352941G>ACA406006205TGFB1,TMEM91c.104C>T (p.Thr35Ile)
c.-30+1739G>A (n.-30+1739G>A)
n.350+1739G>A
 gnomAD v4
19g.41352941G>CCA406006206TGFB1,TMEM91c.104C>G (p.Thr35Ser)
c.-30+1739G>C (n.-30+1739G>C)
n.350+1739G>C
19g.41352941G>TCA406006207TGFB1,TMEM91c.104C>A (p.Thr35Asn)
c.-30+1739G>T (n.-30+1739G>T)
n.350+1739G>T
 gnomAD v4
19g.41352942T>ACA406006208TGFB1,TMEM91c.103A>T (p.Thr35Ser)
c.-30+1740T>A (n.-30+1740T>A)
n.350+1740T>A
19g.41352942T>CCA406006210TGFB1,TMEM91c.103A>G (p.Thr35Ala)
c.-30+1740T>C (n.-30+1740T>C)
n.350+1740T>C
 gnomAD v4
19g.41352942T>GCA406006211TGFB1,TMEM91c.103A>C (p.Thr35Pro)
c.-30+1740T>G (n.-30+1740T>G)
n.350+1740T>G
19g.41352943C>ACA406006213TGFB1,TMEM91c.102G>T (p.Lys34Asn)
c.-30+1741C>A (n.-30+1741C>A)
n.350+1741C>A
 gnomAD v4
19g.41352943C>GCA406006214TGFB1,TMEM91c.102G>C (p.Lys34Asn)
c.-30+1741C>G (n.-30+1741C>G)
n.350+1741C>G
 gnomAD v4
19g.41352943C>TCA507690258TGFB1,TMEM91c.102G>A (p.Lys34=)
c.-30+1741C>T (n.-30+1741C>T)
n.350+1741C>T
 gnomAD v4
19g.41352944T>ACA406006218TGFB1,TMEM91c.101A>T (p.Lys34Met)
c.-30+1742T>A (n.-30+1742T>A)
n.350+1742T>A
 gnomAD v4
19g.41352944T>CCA406006217TGFB1,TMEM91c.101A>G (p.Lys34Arg)
c.-30+1742T>C (n.-30+1742T>C)
n.350+1742T>C
 dbSNP gnomAD v2 gnomAD v4
19g.41352944T>GCA406006216TGFB1,TMEM91c.101A>C (p.Lys34Thr)
c.-30+1742T>G (n.-30+1742T>G)
n.350+1742T>G
19g.41352944T=CA2336426173TGFB1,TMEM91c.101A= (p.Lys34=)
c.-30+1742T= (n.-30+1742T=)
n.350+1742T=
19g.41352945T>ACA406006221TGFB1,TMEM91c.100A>T (p.Lys34Ter)
c.-30+1743T>A (n.-30+1743T>A)
n.350+1743T>A
19g.41352945T>CCA406006219TGFB1,TMEM91c.100A>G (p.Lys34Glu)
c.-30+1743T>C (n.-30+1743T>C)
n.350+1743T>C
 gnomAD v4
19g.41352945T>GCA406006222TGFB1,TMEM91c.100A>C (p.Lys34Gln)
c.-30+1743T>G (n.-30+1743T>G)
n.350+1743T>G
19g.41352946G>ACA507690266TGFB1,TMEM91c.99C>T (p.Cys33=)
c.-30+1744G>A (n.-30+1744G>A)
n.350+1744G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41352946G>CCA406006223TGFB1,TMEM91c.99C>G (p.Cys33Trp)
c.-30+1744G>C (n.-30+1744G>C)
n.350+1744G>C
 gnomAD v4
19g.41352946G=CA2336426174TGFB1,TMEM91c.99C= (p.Cys33=)
c.-30+1744G= (n.-30+1744G=)
n.350+1744G=
19g.41352946G>TCA406006225TGFB1,TMEM91c.99C>A (p.Cys33Ter)
c.-30+1744G>T (n.-30+1744G>T)
n.350+1744G>T
 gnomAD v4
19g.41352947C>ACA406006226TGFB1,TMEM91c.98G>T (p.Cys33Phe)
c.-30+1745C>A (n.-30+1745C>A)
n.350+1745C>A
 gnomAD v4
19g.41352947C>GCA406006228TGFB1,TMEM91c.98G>C (p.Cys33Ser)
c.-30+1745C>G (n.-30+1745C>G)
n.350+1745C>G
19g.41352947C>TCA406006229TGFB1,TMEM91c.98G>A (p.Cys33Tyr)
c.-30+1745C>T (n.-30+1745C>T)
n.350+1745C>T
 gnomAD v4
19g.41352948delCA2585297128TGFB1,TMEM91c.97del (p.Cys33AlafsTer9)
c.-30+1746del (n.-30+1746del)
n.350+1746del
 gnomAD v4
19g.41352948A>CCA406006230TGFB1,TMEM91c.97T>G (p.Cys33Gly)
c.-30+1746A>C (n.-30+1746A>C)
n.350+1746A>C
19g.41352948A>GCA406006231TGFB1,TMEM91c.97T>C (p.Cys33Arg)
c.-30+1746A>G (n.-30+1746A>G)
n.350+1746A>G
 gnomAD v4
19g.41352948A>TCA406006233TGFB1,TMEM91c.97T>A (p.Cys33Ser)
c.-30+1746A>T (n.-30+1746A>T)
n.350+1746A>T
 gnomAD v4
19g.41352949G>ACA507690269TGFB1,TMEM91c.96C>T (p.Thr32=)
c.-30+1747G>A (n.-30+1747G>A)
n.350+1747G>A
19g.41352949G>CCA507690272TGFB1,TMEM91c.96C>G (p.Thr32=)
c.-30+1747G>C (n.-30+1747G>C)
n.350+1747G>C
19g.41352949G=CA2336426175TGFB1,TMEM91c.96C= (p.Thr32=)
c.-30+1747G= (n.-30+1747G=)
n.350+1747G=
19g.41352949G>TCA308518676TGFB1,TMEM91c.96C>A (p.Thr32=)
c.-30+1747G>T (n.-30+1747G>T)
n.350+1747G>T
 dbSNP gnomAD v4
19g.41352950G>ACA406006236TGFB1,TMEM91c.95C>T (p.Thr32Ile)
c.-30+1748G>A (n.-30+1748G>A)
n.350+1748G>A
 gnomAD v4
19g.41352950G>CCA406006237TGFB1,TMEM91c.95C>G (p.Thr32Ser)
c.-30+1748G>C (n.-30+1748G>C)
n.350+1748G>C
19g.41352950G>TCA406006240TGFB1,TMEM91c.95C>A (p.Thr32Asn)
c.-30+1748G>T (n.-30+1748G>T)
n.350+1748G>T
 gnomAD v4
19g.41352951T>ACA406006247TGFB1,TMEM91c.94A>T (p.Thr32Ser)
c.-30+1749T>A (n.-30+1749T>A)
n.350+1749T>A
 gnomAD v4
19g.41352951T>CCA406006245TGFB1,TMEM91c.94A>G (p.Thr32Ala)
c.-30+1749T>C (n.-30+1749T>C)
n.350+1749T>C
 gnomAD v4
19g.41352951T>GCA406006246TGFB1,TMEM91c.94A>C (p.Thr32Pro)
c.-30+1749T>G (n.-30+1749T>G)
n.350+1749T>G
 dbSNP gnomAD v3 gnomAD v4
19g.41352952G>ACA507690275TGFB1,TMEM91c.93C>T (p.Ser31=)
c.-30+1750G>A (n.-30+1750G>A)
n.350+1750G>A
 dbSNP gnomAD v3 gnomAD v4
19g.41352952G>CCA507690276TGFB1,TMEM91c.93C>G (p.Ser31=)
c.-30+1750G>C (n.-30+1750G>C)
n.350+1750G>C
19g.41352952G=CA2336426176TGFB1,TMEM91c.93C= (p.Ser31=)
c.-30+1750G= (n.-30+1750G=)
n.350+1750G=
19g.41352952G>TCA507690277TGFB1,TMEM91c.93C>A (p.Ser31=)
c.-30+1750G>T (n.-30+1750G>T)
n.350+1750G>T
 gnomAD v4
19g.41352953G>ACA406006250TGFB1,TMEM91c.92C>T (p.Ser31Phe)
c.-30+1751G>A (n.-30+1751G>A)
n.350+1751G>A
 gnomAD v4
19g.41352953G>CCA406006251TGFB1,TMEM91c.92C>G (p.Ser31Cys)
c.-30+1751G>C (n.-30+1751G>C)
n.350+1751G>C
 dbSNP gnomAD v2 gnomAD v4
19g.41352953G=CA2336426177TGFB1,TMEM91c.92C= (p.Ser31=)
c.-30+1751G= (n.-30+1751G=)
n.350+1751G=
19g.41352953G>TCA406006254TGFB1,TMEM91c.92C>A (p.Ser31Tyr)
c.-30+1751G>T (n.-30+1751G>T)
n.350+1751G>T
 gnomAD v4
19g.41352954A=CA2336426178TGFB1,TMEM91c.91T= (p.Ser31=)
c.-30+1752A= (n.-30+1752A=)
n.350+1752A=
19g.41352954A>CCA308518678TGFB1,TMEM91c.91T>G (p.Ser31Ala)
c.-30+1752A>C (n.-30+1752A>C)
n.350+1752A>C
 ClinVar dbSNP gnomAD v4
19g.41352954A>GCA406006260TGFB1,TMEM91c.91T>C (p.Ser31Pro)
c.-30+1752A>G (n.-30+1752A>G)
n.350+1752A>G
 dbSNP gnomAD v4
19g.41352954A>TCA406006261TGFB1,TMEM91c.91T>A (p.Ser31Thr)
c.-30+1752A>T (n.-30+1752A>T)
n.350+1752A>T
19g.41352955T>ACA507690283TGFB1,TMEM91c.90A>T (p.Leu30=)
c.-30+1753T>A (n.-30+1753T>A)
n.350+1753T>A
19g.41352955T>CCA507690284TGFB1,TMEM91c.90A>G (p.Leu30=)
c.-30+1753T>C (n.-30+1753T>C)
n.350+1753T>C
 ClinVar dbSNP gnomAD v4
19g.41352955T>GCA507690286TGFB1,TMEM91c.90A>C (p.Leu30=)
c.-30+1753T>G (n.-30+1753T>G)
n.350+1753T>G
19g.41352955T=CA2336426179TGFB1,TMEM91c.90A= (p.Leu30=)
c.-30+1753T= (n.-30+1753T=)
n.350+1753T=
19g.41352956A>CCA406006264TGFB1,TMEM91c.89T>G (p.Leu30Arg)
c.-30+1754A>C (n.-30+1754A>C)
n.350+1754A>C
19g.41352956A>GCA406006265TGFB1,TMEM91c.89T>C (p.Leu30Pro)
c.-30+1754A>G (n.-30+1754A>G)
n.350+1754A>G
19g.41352956A>TCA406006267TGFB1,TMEM91c.89T>A (p.Leu30Gln)
c.-30+1754A>T (n.-30+1754A>T)
n.350+1754A>T
19g.41352957G>ACA507690295TGFB1,TMEM91c.88C>T (p.Leu30=)
c.-30+1755G>A (n.-30+1755G>A)
n.350+1755G>A
 dbSNP gnomAD v2 gnomAD v4
19g.41352957G>CCA406006269TGFB1,TMEM91c.88C>G (p.Leu30Val)
c.-30+1755G>C (n.-30+1755G>C)
n.350+1755G>C
19g.41352957G=CA2336426180TGFB1,TMEM91c.88C= (p.Leu30=)
c.-30+1755G= (n.-30+1755G=)
n.350+1755G=
19g.41352957G>TCA406006271TGFB1,TMEM91c.88C>A (p.Leu30Ile)
c.-30+1755G>T (n.-30+1755G>T)
n.350+1755G>T
 gnomAD v4
19g.41352958T>ACA507690296TGFB1,TMEM91c.87A>T (p.Gly29=)
c.-30+1756T>A (n.-30+1756T>A)
n.350+1756T>A
 dbSNP gnomAD v4
19g.41352958T>CCA507690297TGFB1,TMEM91c.87A>G (p.Gly29=)
c.-30+1756T>C (n.-30+1756T>C)
n.350+1756T>C
 gnomAD v4
19g.41352958T>GCA507690299TGFB1,TMEM91c.87A>C (p.Gly29=)
c.-30+1756T>G (n.-30+1756T>G)
n.350+1756T>G
19g.41352958T=CA2336426181TGFB1,TMEM91c.87A= (p.Gly29=)
c.-30+1756T= (n.-30+1756T=)
n.350+1756T=
19g.41352959C>ACA406006274TGFB1,TMEM91c.86G>T (p.Gly29Val)
c.-30+1757C>A (n.-30+1757C>A)
n.350+1757C>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352959C=CA2336426182TGFB1,TMEM91c.86G= (p.Gly29=)
c.-30+1757C= (n.-30+1757C=)
n.350+1757C=
19g.41352959C>GCA9460174TGFB1,TMEM91c.86G>C (p.Gly29Ala)
c.-30+1757C>G (n.-30+1757C>G)
n.350+1757C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352959C>TCA9460173TGFB1,TMEM91c.86G>A (p.Gly29Glu)
c.-30+1757C>T (n.-30+1757C>T)
n.350+1757C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352961delCA2585297130TGFB1,TMEM91c.86del (p.Gly29AspfsTer13)
c.-30+1759del (n.-30+1759del)
n.350+1759del
 gnomAD v4
19g.41352960_41352961delCA2585297131TGFB1,TMEM91c.85_86del (p.Gly29ThrfsTer?)
c.-30+1758_-30+1759del (n.-30+1758_-30+1759del)
n.350+1758_350+1759del
 gnomAD v4
19g.41352960C>ACA406006279TGFB1,TMEM91c.85G>T (p.Gly29Ter)
c.-30+1758C>A (n.-30+1758C>A)
n.350+1758C>A
 gnomAD v4
19g.41352960C=CA2336426183TGFB1,TMEM91c.85G= (p.Gly29=)
c.-30+1758C= (n.-30+1758C=)
n.350+1758C=
19g.41352960C>GCA308518692TGFB1,TMEM91c.85G>C (p.Gly29Arg)
c.-30+1758C>G (n.-30+1758C>G)
n.350+1758C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352960C>TCA9460175TGFB1,TMEM91c.85G>A (p.Gly29Arg)
c.-30+1758C>T (n.-30+1758C>T)
n.350+1758C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41352961C>ACA507690308TGFB1,TMEM91c.84G>T (p.Ala28=)
c.-30+1759C>A (n.-30+1759C>A)
n.350+1759C>A
 gnomAD v4
19g.41352961C=CA2336426184TGFB1,TMEM91c.84G= (p.Ala28=)
c.-30+1759C= (n.-30+1759C=)
n.350+1759C=
19g.41352961C>GCA507690309TGFB1,TMEM91c.84G>C (p.Ala28=)
c.-30+1759C>G (n.-30+1759C>G)
n.350+1759C>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352961C>TCA308518705TGFB1,TMEM91c.84G>A (p.Ala28=)
c.-30+1759C>T (n.-30+1759C>T)
n.350+1759C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352962G>ACA406006283TGFB1,TMEM91c.83C>T (p.Ala28Val)
c.-30+1760G>A (n.-30+1760G>A)
n.350+1760G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352962G>CCA406006285TGFB1,TMEM91c.83C>G (p.Ala28Gly)
c.-30+1760G>C (n.-30+1760G>C)
n.350+1760G>C
19g.41352962G=CA2336426185TGFB1,TMEM91c.83C= (p.Ala28=)
c.-30+1760G= (n.-30+1760G=)
n.350+1760G=
19g.41352962G>TCA406006287TGFB1,TMEM91c.83C>A (p.Ala28Glu)
c.-30+1760G>T (n.-30+1760G>T)
n.350+1760G>T
 gnomAD v4
19g.41352963C>ACA406006288TGFB1,TMEM91c.82G>T (p.Ala28Ser)
c.-30+1761C>A (n.-30+1761C>A)
n.350+1761C>A
 dbSNP gnomAD v2 gnomAD v4
19g.41352963C=CA2336426186TGFB1,TMEM91c.82G= (p.Ala28=)
c.-30+1761C= (n.-30+1761C=)
n.350+1761C=
19g.41352963C>GCA406006291TGFB1,TMEM91c.82G>C (p.Ala28Pro)
c.-30+1761C>G (n.-30+1761C>G)
n.350+1761C>G
19g.41352963C>TCA406006289TGFB1,TMEM91c.82G>A (p.Ala28Thr)
c.-30+1761C>T (n.-30+1761C>T)
n.350+1761C>T
 gnomAD v4
19g.41352972_41352975delCA2585297132TGFB1,TMEM91c.79_82del (p.Ala27ArgfsTer14)
c.-30+1770_-30+1773del (n.-30+1770_-30+1773del)
n.350+1770_350+1773del
 gnomAD v4
19g.41352964G>ACA507690314TGFB1,TMEM91c.81C>T (p.Ala27=)
c.-30+1762G>A (n.-30+1762G>A)
n.350+1762G>A
 gnomAD v4
19g.41352964G>CCA9460176TGFB1,TMEM91c.81C>G (p.Ala27=)
c.-30+1762G>C (n.-30+1762G>C)
n.350+1762G>C
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41352964G=CA2336426187TGFB1,TMEM91c.81C= (p.Ala27=)
c.-30+1762G= (n.-30+1762G=)
n.350+1762G=
19g.41352964G>TCA507690319TGFB1,TMEM91c.81C>A (p.Ala27=)
c.-30+1762G>T (n.-30+1762G>T)
n.350+1762G>T
 gnomAD v4
19g.41352965G>ACA406006297TGFB1,TMEM91c.80C>T (p.Ala27Val)
c.-30+1763G>A (n.-30+1763G>A)
n.350+1763G>A
 dbSNP gnomAD v2 gnomAD v4
19g.41352965G>CCA406006298TGFB1,TMEM91c.80C>G (p.Ala27Gly)
c.-30+1763G>C (n.-30+1763G>C)
n.350+1763G>C
19g.41352965G=CA2336426188TGFB1,TMEM91c.80C= (p.Ala27=)
c.-30+1763G= (n.-30+1763G=)
n.350+1763G=
19g.41352965G>TCA406006299TGFB1,TMEM91c.80C>A (p.Ala27Asp)
c.-30+1763G>T (n.-30+1763G>T)
n.350+1763G>T
 gnomAD v4
19g.41352966C>ACA406006301TGFB1,TMEM91c.79G>T (p.Ala27Ser)
c.-30+1764C>A (n.-30+1764C>A)
n.350+1764C>A
 gnomAD v4
19g.41352966C=CA2336426189TGFB1,TMEM91c.79G= (p.Ala27=)
c.-30+1764C= (n.-30+1764C=)
n.350+1764C=
19g.41352966C>GCA406006305TGFB1,TMEM91c.79G>C (p.Ala27Pro)
c.-30+1764C>G (n.-30+1764C>G)
n.350+1764C>G
19g.41352966C>TCA406006303TGFB1,TMEM91c.79G>A (p.Ala27Thr)
c.-30+1764C>T (n.-30+1764C>T)
n.350+1764C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352967C>ACA507690323TGFB1,TMEM91c.78G>T (p.Pro26=)
c.-30+1765C>A (n.-30+1765C>A)
n.350+1765C>A
 gnomAD v4
19g.41352967C>GCA507690326TGFB1,TMEM91c.78G>C (p.Pro26=)
c.-30+1765C>G (n.-30+1765C>G)
n.350+1765C>G
19g.41352967C>TCA507690327TGFB1,TMEM91c.78G>A (p.Pro26=)
c.-30+1765C>T (n.-30+1765C>T)
n.350+1765C>T
 gnomAD v4
19g.41352968G>ACA406006306TGFB1,TMEM91c.77C>T (p.Pro26Leu)
c.-30+1766G>A (n.-30+1766G>A)
n.350+1766G>A
 dbSNP gnomAD v3 gnomAD v4
19g.41352968G>CCA406006307TGFB1,TMEM91c.77C>G (p.Pro26Arg)
c.-30+1766G>C (n.-30+1766G>C)
n.350+1766G>C
19g.41352968G=CA2336426190TGFB1,TMEM91c.77C= (p.Pro26=)
c.-30+1766G= (n.-30+1766G=)
n.350+1766G=
19g.41352968G>TCA406006309TGFB1,TMEM91c.77C>A (p.Pro26Gln)
c.-30+1766G>T (n.-30+1766G>T)
n.350+1766G>T
 gnomAD v4
19g.41352969G>ACA406006310TGFB1,TMEM91c.76C>T (p.Pro26Ser)
c.-30+1767G>A (n.-30+1767G>A)
n.350+1767G>A
 dbSNP gnomAD v3 gnomAD v4
19g.41352969G>CCA406006312TGFB1,TMEM91c.76C>G (p.Pro26Ala)
c.-30+1767G>C (n.-30+1767G>C)
n.350+1767G>C
 gnomAD v4
19g.41352969G=CA2336426191TGFB1,TMEM91c.76C= (p.Pro26=)
c.-30+1767G= (n.-30+1767G=)
n.350+1767G=
19g.41352969G>TCA406006314TGFB1,TMEM91c.76C>A (p.Pro26Thr)
c.-30+1767G>T (n.-30+1767G>T)
n.350+1767G>T
 gnomAD v4
19g.41352970C>ACA507690339TGFB1,TMEM91c.75G>T (p.Arg25=)
c.-30+1768C>A (n.-30+1768C>A)
n.350+1768C>A
 gnomAD v4
19g.41352970C=CA2336426192TGFB1,TMEM91c.75G= (p.Arg25=)
c.-30+1768C= (n.-30+1768C=)
n.350+1768C=
19g.41352970C>GCA507690338TGFB1,TMEM91c.75G>C (p.Arg25=)
c.-30+1768C>G (n.-30+1768C>G)
n.350+1768C>G
19g.41352970C>TCA507690335TGFB1,TMEM91c.75G>A (p.Arg25=)
c.-30+1768C>T (n.-30+1768C>T)
n.350+1768C>T
 dbSNP gnomAD v4
19g.41352971C>ACA406006316TGFB1,TMEM91c.74G>T (p.Arg25Leu)
c.-30+1769C>A (n.-30+1769C>A)
n.350+1769C>A
 gnomAD v4
19g.41352971C=CA2336426193TGFB1,TMEM91c.74G= (p.Arg25=)
c.-30+1769C= (n.-30+1769C=)
n.350+1769C=
19g.41352971C>GCA9460177TGFB1,TMEM91c.74G>C (p.Arg25Pro)
c.-30+1769C>G (n.-30+1769C>G)
n.350+1769C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352971C>TCA406006321TGFB1,TMEM91c.74G>A (p.Arg25Gln)
c.-30+1769C>T (n.-30+1769C>T)
n.350+1769C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352972G>ACA406006326TGFB1,TMEM91c.73C>T (p.Arg25Trp)
c.-30+1770G>A (n.-30+1770G>A)
n.350+1770G>A
 dbSNP gnomAD v2 gnomAD v4
19g.41352972G>CCA406006328TGFB1,TMEM91c.73C>G (p.Arg25Gly)
c.-30+1770G>C (n.-30+1770G>C)
n.350+1770G>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41352972G=CA2336426194TGFB1,TMEM91c.73C= (p.Arg25=)
c.-30+1770G= (n.-30+1770G=)
n.350+1770G=
19g.41352972G>TCA507690344TGFB1,TMEM91c.73C>A (p.Arg25=)
c.-30+1770G>T (n.-30+1770G>T)
n.350+1770G>T
 dbSNP gnomAD v4
19g.41352973G>ACA507690345TGFB1,TMEM91c.72C>T (p.Gly24=)
c.-30+1771G>A (n.-30+1771G>A)
n.350+1771G>A
 gnomAD v4
19g.41352973G>CCA507690346TGFB1,TMEM91c.72C>G (p.Gly24=)
c.-30+1771G>C (n.-30+1771G>C)
n.350+1771G>C
19g.41352973G=CA2336426195TGFB1,TMEM91c.72C= (p.Gly24=)
c.-30+1771G= (n.-30+1771G=)
n.350+1771G=
19g.41352973G>TCA9460178TGFB1,TMEM91c.72C>A (p.Gly24=)
c.-30+1771G>T (n.-30+1771G>T)
n.350+1771G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352974C>ACA406006332TGFB1,TMEM91c.71G>T (p.Gly24Val)
c.-30+1772C>A (n.-30+1772C>A)
n.350+1772C>A
 gnomAD v4
19g.41352974C=CA2336426196TGFB1,TMEM91c.71G= (p.Gly24=)
c.-30+1772C= (n.-30+1772C=)
n.350+1772C=
19g.41352974C>GCA406006334TGFB1,TMEM91c.71G>C (p.Gly24Ala)
c.-30+1772C>G (n.-30+1772C>G)
n.350+1772C>G
19g.41352974C>TCA406006330TGFB1,TMEM91c.71G>A (p.Gly24Asp)
c.-30+1772C>T (n.-30+1772C>T)
n.350+1772C>T
 dbSNP gnomAD v2 gnomAD v4
19g.41352978_41352990delCA2585297133TGFB1,TMEM91c.59_71del (p.Val20AlafsTer18)
c.-30+1776_-30+1788del (n.-30+1776_-30+1788del)
n.350+1776_350+1788del
 gnomAD v4
19g.41352975C>ACA406006335TGFB1,TMEM91c.70G>T (p.Gly24Cys)
c.-30+1773C>A (n.-30+1773C>A)
n.350+1773C>A
 gnomAD v4
19g.41352975C=CA2336426197TGFB1,TMEM91c.70G= (p.Gly24=)
c.-30+1773C= (n.-30+1773C=)
n.350+1773C=
19g.41352975C>GCA406006340TGFB1,TMEM91c.70G>C (p.Gly24Arg)
c.-30+1773C>G (n.-30+1773C>G)
n.350+1773C>G
 gnomAD v4
19g.41352975C>TCA406006337TGFB1,TMEM91c.70G>A (p.Gly24Ser)
c.-30+1773C>T (n.-30+1773C>T)
n.350+1773C>T
 dbSNP gnomAD v3 gnomAD v4
19g.41352976A>CCA507690350TGFB1,TMEM91c.69T>G (p.Pro23=)
c.-30+1774A>C (n.-30+1774A>C)
n.350+1774A>C
19g.41352976A>GCA507690354TGFB1,TMEM91c.69T>C (p.Pro23=)
c.-30+1774A>G (n.-30+1774A>G)
n.350+1774A>G
 gnomAD v4
19g.41352976A>TCA507690352TGFB1,TMEM91c.69T>A (p.Pro23=)
c.-30+1774A>T (n.-30+1774A>T)
n.350+1774A>T
19g.41352977G>ACA406006342TGFB1,TMEM91c.68C>T (p.Pro23Leu)
c.-30+1775G>A (n.-30+1775G>A)
n.350+1775G>A
 dbSNP
19g.41352977G>CCA406006348TGFB1,TMEM91c.68C>G (p.Pro23Arg)
c.-30+1775G>C (n.-30+1775G>C)
n.350+1775G>C
19g.41352977G>TCA406006346TGFB1,TMEM91c.68C>A (p.Pro23His)
c.-30+1775G>T (n.-30+1775G>T)
n.350+1775G>T
 gnomAD v4
19g.41352978G>ACA406006349TGFB1,TMEM91c.67C>T (p.Pro23Ser)
c.-30+1776G>A (n.-30+1776G>A)
n.350+1776G>A
 gnomAD v4
19g.41352978G>CCA406006351TGFB1,TMEM91c.67C>G (p.Pro23Ala)
c.-30+1776G>C (n.-30+1776G>C)
n.350+1776G>C
 gnomAD v4
19g.41352978G>TCA406006353TGFB1,TMEM91c.67C>A (p.Pro23Thr)
c.-30+1776G>T (n.-30+1776G>T)
n.350+1776G>T
 gnomAD v4
19g.41352979C>ACA507690362TGFB1,TMEM91c.66G>T (p.Thr22=)
c.-30+1777C>A (n.-30+1777C>A)
n.350+1777C>A
 gnomAD v4
19g.41352979C>GCA507690364TGFB1,TMEM91c.66G>C (p.Thr22=)
c.-30+1777C>G (n.-30+1777C>G)
n.350+1777C>G
 gnomAD v4
19g.41352979C>TCA507690366TGFB1,TMEM91c.66G>A (p.Thr22=)
c.-30+1777C>T (n.-30+1777C>T)
n.350+1777C>T
 gnomAD v4
19g.41352980G>ACA406006355TGFB1,TMEM91c.65C>T (p.Thr22Met)
c.-30+1778G>A (n.-30+1778G>A)
n.350+1778G>A
 gnomAD v4
19g.41352980G>CCA406006356TGFB1,TMEM91c.65C>G (p.Thr22Arg)
c.-30+1778G>C (n.-30+1778G>C)
n.350+1778G>C
 gnomAD v4
19g.41352980G>TCA406006357TGFB1,TMEM91c.65C>A (p.Thr22Lys)
c.-30+1778G>T (n.-30+1778G>T)
n.350+1778G>T
 gnomAD v4
19g.41352981T>ACA406006362TGFB1,TMEM91c.64A>T (p.Thr22Ser)
c.-30+1779T>A (n.-30+1779T>A)
n.350+1779T>A
 dbSNP gnomAD v3 gnomAD v4
19g.41352981T>CCA406006364TGFB1,TMEM91c.64A>G (p.Thr22Ala)
c.-30+1779T>C (n.-30+1779T>C)
n.350+1779T>C
19g.41352981T>GCA406006365TGFB1,TMEM91c.64A>C (p.Thr22Pro)
c.-30+1779T>G (n.-30+1779T>G)
n.350+1779T>G
 dbSNP gnomAD v4
19g.41352981T=CA2336426198TGFB1,TMEM91c.64A= (p.Thr22=)
c.-30+1779T= (n.-30+1779T=)
n.350+1779T=
19g.41352982C>ACA507690378TGFB1,TMEM91c.63G>T (p.Leu21=)
c.-30+1780C>A (n.-30+1780C>A)
n.350+1780C>A
 gnomAD v4
19g.41352982C>GCA507690382TGFB1,TMEM91c.63G>C (p.Leu21=)
c.-30+1780C>G (n.-30+1780C>G)
n.350+1780C>G
19g.41352982C>TCA507690381TGFB1,TMEM91c.63G>A (p.Leu21=)
c.-30+1780C>T (n.-30+1780C>T)
n.350+1780C>T
 gnomAD v4
19g.41352983A=CA2336426199TGFB1,TMEM91c.62T= (p.Leu21=)
c.-30+1781A= (n.-30+1781A=)
n.350+1781A=
19g.41352983A>CCA406006366TGFB1,TMEM91c.62T>G (p.Leu21Arg)
c.-30+1781A>C (n.-30+1781A>C)
n.350+1781A>C
19g.41352983A>GCA9460179TGFB1,TMEM91c.62T>C (p.Leu21Pro)
c.-30+1781A>G (n.-30+1781A>G)
n.350+1781A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41352983A>TCA406006367TGFB1,TMEM91c.62T>A (p.Leu21Gln)
c.-30+1781A>T (n.-30+1781A>T)
n.350+1781A>T
 gnomAD v4
19g.41352984G>ACA507690386TGFB1,TMEM91c.61C>T (p.Leu21=)
c.-30+1782G>A (n.-30+1782G>A)
n.350+1782G>A
 gnomAD v4
19g.41352984G>CCA406006369TGFB1,TMEM91c.61C>G (p.Leu21Val)
c.-30+1782G>C (n.-30+1782G>C)
n.350+1782G>C
19g.41352984G>TCA406006371TGFB1,TMEM91c.61C>A (p.Leu21Met)
c.-30+1782G>T (n.-30+1782G>T)
n.350+1782G>T
 gnomAD v4
19g.41352985C>ACA507690389TGFB1,TMEM91c.60G>T (p.Val20=)
c.-30+1783C>A (n.-30+1783C>A)
n.350+1783C>A
 gnomAD v4
19g.41352985C=CA2336426200TGFB1,TMEM91c.60G= (p.Val20=)
c.-30+1783C= (n.-30+1783C=)
n.350+1783C=
19g.41352985C>GCA507690390TGFB1,TMEM91c.60G>C (p.Val20=)
c.-30+1783C>G (n.-30+1783C>G)
n.350+1783C>G
19g.41352985C>TCA507690392TGFB1,TMEM91c.60G>A (p.Val20=)
c.-30+1783C>T (n.-30+1783C>T)
n.350+1783C>T
 dbSNP gnomAD v2 gnomAD v4
19g.41352986A>CCA406006373TGFB1,TMEM91c.59T>G (p.Val20Gly)
c.-30+1784A>C (n.-30+1784A>C)
n.350+1784A>C
 gnomAD v4
19g.41352986A>GCA406006374TGFB1,TMEM91c.59T>C (p.Val20Ala)
c.-30+1784A>G (n.-30+1784A>G)
n.350+1784A>G
 gnomAD v4
19g.41352986A>TCA406006376TGFB1,TMEM91c.59T>A (p.Val20Glu)
c.-30+1784A>T (n.-30+1784A>T)
n.350+1784A>T
19g.41352987C>ACA406006378TGFB1,TMEM91c.58G>T (p.Val20Leu)
c.-30+1785C>A (n.-30+1785C>A)
n.350+1785C>A
 gnomAD v4
19g.41352987C=CA2336426201TGFB1,TMEM91c.58G= (p.Val20=)
c.-30+1785C= (n.-30+1785C=)
n.350+1785C=
19g.41352987C>GCA9460180TGFB1,TMEM91c.58G>C (p.Val20Leu)
c.-30+1785C>G (n.-30+1785C>G)
n.350+1785C>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352987C>TCA406006380TGFB1,TMEM91c.58G>A (p.Val20Met)
c.-30+1785C>T (n.-30+1785C>T)
n.350+1785C>T
 gnomAD v4
19g.41352988delCA2585297134TGFB1,TMEM91c.58del (p.Val20CysfsTer2)
c.-30+1786del (n.-30+1786del)
n.350+1786del
 gnomAD v4
19g.41352988C>ACA507690398TGFB1,TMEM91c.57G>T (p.Leu19=)
c.-30+1786C>A (n.-30+1786C>A)
n.350+1786C>A
 gnomAD v4
19g.41352988C>GCA507690399TGFB1,TMEM91c.57G>C (p.Leu19=)
c.-30+1786C>G (n.-30+1786C>G)
n.350+1786C>G
19g.41352988C>TCA507690400TGFB1,TMEM91c.57G>A (p.Leu19=)
c.-30+1786C>T (n.-30+1786C>T)
n.350+1786C>T
 gnomAD v4
19g.41352989A=CA2336426202TGFB1,TMEM91c.56T= (p.Leu19=)
c.-30+1787A= (n.-30+1787A=)
n.350+1787A=
19g.41352989A>CCA406006382TGFB1,TMEM91c.56T>G (p.Leu19Arg)
c.-30+1787A>C (n.-30+1787A>C)
n.350+1787A>C
 dbSNP gnomAD v2 gnomAD v4
19g.41352989A>GCA308518726TGFB1,TMEM91c.56T>C (p.Leu19Pro)
c.-30+1787A>G (n.-30+1787A>G)
n.350+1787A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352989A>TCA406006384TGFB1,TMEM91c.56T>A (p.Leu19Gln)
c.-30+1787A>T (n.-30+1787A>T)
n.350+1787A>T
 gnomAD v4
19g.41352990G>ACA9460181TGFB1,TMEM91c.55C>T (p.Leu19=)
c.-30+1788G>A (n.-30+1788G>A)
n.350+1788G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352990G>CCA406006387TGFB1,TMEM91c.55C>G (p.Leu19Val)
c.-30+1788G>C (n.-30+1788G>C)
n.350+1788G>C
 gnomAD v4
19g.41352990G=CA2336426203TGFB1,TMEM91c.55C= (p.Leu19=)
c.-30+1788G= (n.-30+1788G=)
n.350+1788G=
19g.41352990G>TCA308518737TGFB1,TMEM91c.55C>A (p.Leu19Met)
c.-30+1788G>T (n.-30+1788G>T)
n.350+1788G>T
 dbSNP gnomAD v4
19g.41352991T>ACA507690412TGFB1,TMEM91c.54A>T (p.Leu18=)
c.-30+1789T>A (n.-30+1789T>A)
n.350+1789T>A
19g.41352991T>CCA507690406TGFB1,TMEM91c.54A>G (p.Leu18=)
c.-30+1789T>C (n.-30+1789T>C)
n.350+1789T>C
 gnomAD v4
19g.41352991T>GCA507690409TGFB1,TMEM91c.54A>C (p.Leu18=)
c.-30+1789T>G (n.-30+1789T>G)
n.350+1789T>G

Number of alleles fetched