Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.41352770C>ACA406005153TGFB1,TMEM91c.275G>T (p.Ser92Ile)
c.-30+1568C>A (n.-30+1568C>A)
n.350+1568C>A
19g.41352770C>GCA406005154TGFB1,TMEM91c.275G>C (p.Ser92Thr)
c.-30+1568C>G (n.-30+1568C>G)
n.350+1568C>G
19g.41352770C>TCA406005156TGFB1,TMEM91c.275G>A (p.Ser92Asn)
c.-30+1568C>T (n.-30+1568C>T)
n.350+1568C>T
 COSMIC
19g.41352773_41352774dupCA2336426093TGFB1,TMEM91c.274_275dup (p.Ser92ArgfsTer22)
c.-30+1571_-30+1572dup (n.-30+1571_-30+1572dup)
n.350+1571_350+1572dup
 ClinVar dbSNP
19g.41352771T>ACA406005161TGFB1,TMEM91c.274A>T (p.Ser92Cys)
c.-30+1569T>A (n.-30+1569T>A)
n.350+1569T>A
19g.41352771T>CCA406005159TGFB1,TMEM91c.274A>G (p.Ser92Gly)
c.-30+1569T>C (n.-30+1569T>C)
n.350+1569T>C
19g.41352771T>GCA406005158TGFB1,TMEM91c.274A>C (p.Ser92Arg)
c.-30+1569T>G (n.-30+1569T>G)
n.350+1569T>G
19g.41352772C>ACA406005163TGFB1,TMEM91c.273G>T (p.Glu91Asp)
c.-30+1570C>A (n.-30+1570C>A)
n.350+1570C>A
19g.41352772C>GCA406005165TGFB1,TMEM91c.273G>C (p.Glu91Asp)
c.-30+1570C>G (n.-30+1570C>G)
n.350+1570C>G
19g.41352772C>TCA507690010TGFB1,TMEM91c.273G>A (p.Glu91=)
c.-30+1570C>T (n.-30+1570C>T)
n.350+1570C>T
19g.41352773T>ACA406005167TGFB1,TMEM91c.272A>T (p.Glu91Val)
c.-30+1571T>A (n.-30+1571T>A)
n.350+1571T>A
19g.41352773T>CCA406005168TGFB1,TMEM91c.272A>G (p.Glu91Gly)
c.-30+1571T>C (n.-30+1571T>C)
n.350+1571T>C
 ClinVar dbSNP gnomAD v4
19g.41352773T>GCA406005169TGFB1,TMEM91c.272A>C (p.Glu91Ala)
c.-30+1571T>G (n.-30+1571T>G)
n.350+1571T>G
19g.41352773T=CA2336426094TGFB1,TMEM91c.272A= (p.Glu91=)
c.-30+1571T= (n.-30+1571T=)
n.350+1571T=
19g.41352774C>ACA406005172TGFB1,TMEM91c.271G>T (p.Glu91Ter)
c.-30+1572C>A (n.-30+1572C>A)
n.350+1572C>A
19g.41352774C=CA2336426095TGFB1,TMEM91c.271G= (p.Glu91=)
c.-30+1572C= (n.-30+1572C=)
n.350+1572C=
19g.41352774C>GCA406005173TGFB1,TMEM91c.271G>C (p.Glu91Gln)
c.-30+1572C>G (n.-30+1572C>G)
n.350+1572C>G
19g.41352774C>TCA406005175TGFB1,TMEM91c.271G>A (p.Glu91Lys)
c.-30+1572C>T (n.-30+1572C>T)
n.350+1572C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41352777dupCA2585297350TGFB1,TMEM91c.271dup (p.Glu91GlyfsTer10)
c.-30+1575dup (n.-30+1575dup)
n.350+1575dup
 gnomAD v4
19g.41352777delCA2585297351TGFB1,TMEM91c.271del (p.Glu91ArgfsTer22)
c.-30+1575del (n.-30+1575del)
n.350+1575del
 gnomAD v4
19g.41352775C>ACA507690025TGFB1,TMEM91c.270G>T (p.Gly90=)
c.-30+1573C>A (n.-30+1573C>A)
n.350+1573C>A
19g.41352775C=CA2336426096TGFB1,TMEM91c.270G= (p.Gly90=)
c.-30+1573C= (n.-30+1573C=)
n.350+1573C=
19g.41352775C>GCA507690017TGFB1,TMEM91c.270G>C (p.Gly90=)
c.-30+1573C>G (n.-30+1573C>G)
n.350+1573C>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352775C>TCA507690024TGFB1,TMEM91c.270G>A (p.Gly90=)
c.-30+1573C>T (n.-30+1573C>T)
n.350+1573C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352776C>ACA406005183TGFB1,TMEM91c.269G>T (p.Gly90Val)
c.-30+1574C>A (n.-30+1574C>A)
n.350+1574C>A
19g.41352776C=CA2336426097TGFB1,TMEM91c.269G= (p.Gly90=)
c.-30+1574C= (n.-30+1574C=)
n.350+1574C=
19g.41352776C>GCA406005184TGFB1,TMEM91c.269G>C (p.Gly90Ala)
c.-30+1574C>G (n.-30+1574C>G)
n.350+1574C>G
19g.41352776C>TCA406005185TGFB1,TMEM91c.269G>A (p.Gly90Glu)
c.-30+1574C>T (n.-30+1574C>T)
n.350+1574C>T
 dbSNP gnomAD v2
19g.41352777C>ACA406005186TGFB1,TMEM91c.268G>T (p.Gly90Trp)
c.-30+1575C>A (n.-30+1575C>A)
n.350+1575C>A
19g.41352777C=CA2336426098TGFB1,TMEM91c.268G= (p.Gly90=)
c.-30+1575C= (n.-30+1575C=)
n.350+1575C=
19g.41352777C>GCA406005187TGFB1,TMEM91c.268G>C (p.Gly90Arg)
c.-30+1575C>G (n.-30+1575C>G)
n.350+1575C>G
19g.41352777C>TCA406005191TGFB1,TMEM91c.268G>A (p.Gly90Arg)
c.-30+1575C>T (n.-30+1575C>T)
n.350+1575C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352778G>ACA507690034TGFB1,TMEM91c.267C>T (p.Ala89=)
c.-30+1576G>A (n.-30+1576G>A)
n.350+1576G>A
19g.41352778G>CCA507690036TGFB1,TMEM91c.267C>G (p.Ala89=)
c.-30+1576G>C (n.-30+1576G>C)
n.350+1576G>C
19g.41352778G=CA2336426099TGFB1,TMEM91c.267C= (p.Ala89=)
c.-30+1576G= (n.-30+1576G=)
n.350+1576G=
19g.41352778G>TCA507690037TGFB1,TMEM91c.267C>A (p.Ala89=)
c.-30+1576G>T (n.-30+1576G>T)
n.350+1576G>T
 dbSNP gnomAD v2
19g.41352779G>ACA9460152TGFB1,TMEM91c.266C>T (p.Ala89Val)
c.-30+1577G>A (n.-30+1577G>A)
n.350+1577G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352779G>CCA406005193TGFB1,TMEM91c.266C>G (p.Ala89Gly)
c.-30+1577G>C (n.-30+1577G>C)
n.350+1577G>C
19g.41352779G=CA2336426100TGFB1,TMEM91c.266C= (p.Ala89=)
c.-30+1577G= (n.-30+1577G=)
n.350+1577G=
19g.41352779G>TCA406005194TGFB1,TMEM91c.266C>A (p.Ala89Asp)
c.-30+1577G>T (n.-30+1577G>T)
n.350+1577G>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352780C>ACA406005198TGFB1,TMEM91c.265G>T (p.Ala89Ser)
c.-30+1578C>A (n.-30+1578C>A)
n.350+1578C>A
19g.41352780C>GCA406005199TGFB1,TMEM91c.265G>C (p.Ala89Pro)
c.-30+1578C>G (n.-30+1578C>G)
n.350+1578C>G
19g.41352780C>TCA406005201TGFB1,TMEM91c.265G>A (p.Ala89Thr)
c.-30+1578C>T (n.-30+1578C>T)
n.350+1578C>T
19g.41352781C>ACA507690044TGFB1,TMEM91c.264G>T (p.Val88=)
c.-30+1579C>A (n.-30+1579C>A)
n.350+1579C>A
19g.41352781C>GCA507690045TGFB1,TMEM91c.264G>C (p.Val88=)
c.-30+1579C>G (n.-30+1579C>G)
n.350+1579C>G
19g.41352781C>TCA507690048TGFB1,TMEM91c.264G>A (p.Val88=)
c.-30+1579C>T (n.-30+1579C>T)
n.350+1579C>T
19g.41352782A>CCA406005202TGFB1,TMEM91c.263T>G (p.Val88Gly)
c.-30+1580A>C (n.-30+1580A>C)
n.350+1580A>C
19g.41352782A>GCA406005203TGFB1,TMEM91c.263T>C (p.Val88Ala)
c.-30+1580A>G (n.-30+1580A>G)
n.350+1580A>G
19g.41352782A>TCA406005205TGFB1,TMEM91c.263T>A (p.Val88Glu)
c.-30+1580A>T (n.-30+1580A>T)
n.350+1580A>T
19g.41352783C>ACA406005206TGFB1,TMEM91c.262G>T (p.Val88Leu)
c.-30+1581C>A (n.-30+1581C>A)
n.350+1581C>A
19g.41352783C>GCA406005207TGFB1,TMEM91c.262G>C (p.Val88Leu)
c.-30+1581C>G (n.-30+1581C>G)
n.350+1581C>G
19g.41352783C>TCA406005208TGFB1,TMEM91c.262G>A (p.Val88Met)
c.-30+1581C>T (n.-30+1581C>T)
n.350+1581C>T
19g.41352784C>ACA507690052TGFB1,TMEM91c.261G>T (p.Arg87=)
c.-30+1582C>A (n.-30+1582C>A)
n.350+1582C>A
 gnomAD v4
19g.41352784C=CA2336426101TGFB1,TMEM91c.261G= (p.Arg87=)
c.-30+1582C= (n.-30+1582C=)
n.350+1582C=
19g.41352784C>GCA507690053TGFB1,TMEM91c.261G>C (p.Arg87=)
c.-30+1582C>G (n.-30+1582C>G)
n.350+1582C>G
 gnomAD v4
19g.41352784C>TCA507690055TGFB1,TMEM91c.261G>A (p.Arg87=)
c.-30+1582C>T (n.-30+1582C>T)
n.350+1582C>T
 dbSNP gnomAD v4
19g.41352785C>ACA406005209TGFB1,TMEM91c.260G>T (p.Arg87Leu)
c.-30+1583C>A (n.-30+1583C>A)
n.350+1583C>A
 gnomAD v4
19g.41352785C=CA2336426102TGFB1,TMEM91c.260G= (p.Arg87=)
c.-30+1583C= (n.-30+1583C=)
n.350+1583C=
19g.41352785C>GCA9460153TGFB1,TMEM91c.260G>C (p.Arg87Pro)
c.-30+1583C>G (n.-30+1583C>G)
n.350+1583C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41352785C>TCA406005210TGFB1,TMEM91c.260G>A (p.Arg87Gln)
c.-30+1583C>T (n.-30+1583C>T)
n.350+1583C>T
19g.41352786G>ACA406005213TGFB1,TMEM91c.259C>T (p.Arg87Trp)
c.-30+1584G>A (n.-30+1584G>A)
n.350+1584G>A
 gnomAD v4
19g.41352786G>CCA406005211TGFB1,TMEM91c.259C>G (p.Arg87Gly)
c.-30+1584G>C (n.-30+1584G>C)
n.350+1584G>C
19g.41352786G>TCA507690060TGFB1,TMEM91c.259C>A (p.Arg87=)
c.-30+1584G>T (n.-30+1584G>T)
n.350+1584G>T
19g.41352787G>ACA9460154TGFB1,TMEM91c.258C>T (p.Asp86=)
c.-30+1585G>A (n.-30+1585G>A)
n.350+1585G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41352787G>CCA406005214TGFB1,TMEM91c.258C>G (p.Asp86Glu)
c.-30+1585G>C (n.-30+1585G>C)
n.350+1585G>C
19g.41352787G=CA2336426103TGFB1,TMEM91c.258C= (p.Asp86=)
c.-30+1585G= (n.-30+1585G=)
n.350+1585G=
19g.41352787G>TCA406005215TGFB1,TMEM91c.258C>A (p.Asp86Glu)
c.-30+1585G>T (n.-30+1585G>T)
n.350+1585G>T
 ClinVar gnomAD v4
19g.41352788T>ACA406005217TGFB1,TMEM91c.257A>T (p.Asp86Val)
c.-30+1586T>A (n.-30+1586T>A)
n.350+1586T>A
19g.41352788T>CCA406005219TGFB1,TMEM91c.257A>G (p.Asp86Gly)
c.-30+1586T>C (n.-30+1586T>C)
n.350+1586T>C
19g.41352788T>GCA406005220TGFB1,TMEM91c.257A>C (p.Asp86Ala)
c.-30+1586T>G (n.-30+1586T>G)
n.350+1586T>G
19g.41352789C>ACA9460155TGFB1,TMEM91c.256G>T (p.Asp86Tyr)
c.-30+1587C>A (n.-30+1587C>A)
n.350+1587C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352789C=CA2336426104TGFB1,TMEM91c.256G= (p.Asp86=)
c.-30+1587C= (n.-30+1587C=)
n.350+1587C=
19g.41352789C>GCA406005223TGFB1,TMEM91c.256G>C (p.Asp86His)
c.-30+1587C>G (n.-30+1587C>G)
n.350+1587C>G
 ClinVar dbSNP gnomAD v4
19g.41352789C>TCA406005225TGFB1,TMEM91c.256G>A (p.Asp86Asn)
c.-30+1587C>T (n.-30+1587C>T)
n.350+1587C>T
19g.41352790G>ACA9460156TGFB1,TMEM91c.255C>T (p.Arg85=)
c.-30+1588G>A (n.-30+1588G>A)
n.350+1588G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352790G>CCA507690069TGFB1,TMEM91c.255C>G (p.Arg85=)
c.-30+1588G>C (n.-30+1588G>C)
n.350+1588G>C
19g.41352790G=CA2336426105TGFB1,TMEM91c.255C= (p.Arg85=)
c.-30+1588G= (n.-30+1588G=)
n.350+1588G=
19g.41352790G>TCA507690071TGFB1,TMEM91c.255C>A (p.Arg85=)
c.-30+1588G>T (n.-30+1588G>T)
n.350+1588G>T
19g.41352791C>ACA406005228TGFB1,TMEM91c.254G>T (p.Arg85Leu)
c.-30+1589C>A (n.-30+1589C>A)
n.350+1589C>A
19g.41352791C>GCA406005231TGFB1,TMEM91c.254G>C (p.Arg85Pro)
c.-30+1589C>G (n.-30+1589C>G)
n.350+1589C>G
 gnomAD v4
19g.41352791C>TCA406005234TGFB1,TMEM91c.254G>A (p.Arg85His)
c.-30+1589C>T (n.-30+1589C>T)
n.350+1589C>T
19g.41352792G>ACA406005240TGFB1,TMEM91c.253C>T (p.Arg85Cys)
c.-30+1590G>A (n.-30+1590G>A)
n.350+1590G>A
 ClinVar
19g.41352792G>CCA406005241TGFB1,TMEM91c.253C>G (p.Arg85Gly)
c.-30+1590G>C (n.-30+1590G>C)
n.350+1590G>C
 gnomAD v4
19g.41352792G>TCA406005237TGFB1,TMEM91c.253C>A (p.Arg85Ser)
c.-30+1590G>T (n.-30+1590G>T)
n.350+1590G>T
19g.41352793G>ACA9460157TGFB1,TMEM91c.252C>T (p.Thr84=)
c.-30+1591G>A (n.-30+1591G>A)
n.350+1591G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41352793G>CCA507690077TGFB1,TMEM91c.252C>G (p.Thr84=)
c.-30+1591G>C (n.-30+1591G>C)
n.350+1591G>C
19g.41352793G=CA2336426106TGFB1,TMEM91c.252C= (p.Thr84=)
c.-30+1591G= (n.-30+1591G=)
n.350+1591G=
19g.41352793G>TCA308518504TGFB1,TMEM91c.252C>A (p.Thr84=)
c.-30+1591G>T (n.-30+1591G>T)
n.350+1591G>T
 dbSNP
19g.41352794G>ACA406005248TGFB1,TMEM91c.251C>T (p.Thr84Ile)
c.-30+1592G>A (n.-30+1592G>A)
n.350+1592G>A
19g.41352794G>CCA406005249TGFB1,TMEM91c.251C>G (p.Thr84Ser)
c.-30+1592G>C (n.-30+1592G>C)
n.350+1592G>C
19g.41352794G>TCA406005252TGFB1,TMEM91c.251C>A (p.Thr84Asn)
c.-30+1592G>T (n.-30+1592G>T)
n.350+1592G>T
19g.41352795T>ACA406005260TGFB1,TMEM91c.250A>T (p.Thr84Ser)
c.-30+1593T>A (n.-30+1593T>A)
n.350+1593T>A
 dbSNP gnomAD v4
19g.41352795T>CCA406005256TGFB1,TMEM91c.250A>G (p.Thr84Ala)
c.-30+1593T>C (n.-30+1593T>C)
n.350+1593T>C
19g.41352795T>GCA406005258TGFB1,TMEM91c.250A>C (p.Thr84Pro)
c.-30+1593T>G (n.-30+1593T>G)
n.350+1593T>G
19g.41352795T=CA2336426107TGFB1,TMEM91c.250A= (p.Thr84=)
c.-30+1593T= (n.-30+1593T=)
n.350+1593T=
19g.41352796G>ACA507690079TGFB1,TMEM91c.249C>T (p.Ser83=)
c.-30+1594G>A (n.-30+1594G>A)
n.350+1594G>A
 gnomAD v4
19g.41352796G>CCA406005262TGFB1,TMEM91c.249C>G (p.Ser83Arg)
c.-30+1594G>C (n.-30+1594G>C)
n.350+1594G>C
19g.41352796G>TCA406005270TGFB1,TMEM91c.249C>A (p.Ser83Arg)
c.-30+1594G>T (n.-30+1594G>T)
n.350+1594G>T
 gnomAD v4
19g.41352797C>ACA406005272TGFB1,TMEM91c.248G>T (p.Ser83Ile)
c.-30+1595C>A (n.-30+1595C>A)
n.350+1595C>A
 COSMIC
19g.41352797C=CA2336426108TGFB1,TMEM91c.248G= (p.Ser83=)
c.-30+1595C= (n.-30+1595C=)
n.350+1595C=
19g.41352797C>GCA9460158TGFB1,TMEM91c.248G>C (p.Ser83Thr)
c.-30+1595C>G (n.-30+1595C>G)
n.350+1595C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352797C>TCA406005276TGFB1,TMEM91c.248G>A (p.Ser83Asn)
c.-30+1595C>T (n.-30+1595C>T)
n.350+1595C>T
 gnomAD v4
19g.41352798T>ACA406005278TGFB1,TMEM91c.247A>T (p.Ser83Cys)
c.-30+1596T>A (n.-30+1596T>A)
n.350+1596T>A
19g.41352798T>CCA406005283TGFB1,TMEM91c.247A>G (p.Ser83Gly)
c.-30+1596T>C (n.-30+1596T>C)
n.350+1596T>C
19g.41352798T>GCA406005280TGFB1,TMEM91c.247A>C (p.Ser83Arg)
c.-30+1596T>G (n.-30+1596T>G)
n.350+1596T>G
19g.41352801_41352803delCA645607130TGFB1,TMEM91c.245_247del (p.Asn82del)
c.-30+1599_-30+1601del (n.-30+1599_-30+1601del)
n.350+1599_350+1601del
 COSMIC
19g.41352799G>ACA507690086TGFB1,TMEM91c.246C>T (p.Asn82=)
c.-30+1597G>A (n.-30+1597G>A)
n.350+1597G>A
19g.41352799G>CCA406005285TGFB1,TMEM91c.246C>G (p.Asn82Lys)
c.-30+1597G>C (n.-30+1597G>C)
n.350+1597G>C
19g.41352799G>TCA406005288TGFB1,TMEM91c.246C>A (p.Asn82Lys)
c.-30+1597G>T (n.-30+1597G>T)
n.350+1597G>T
 gnomAD v4
19g.41352800T>ACA406005290TGFB1,TMEM91c.245A>T (p.Asn82Ile)
c.-30+1598T>A (n.-30+1598T>A)
n.350+1598T>A
19g.41352800T>CCA406005294TGFB1,TMEM91c.245A>G (p.Asn82Ser)
c.-30+1598T>C (n.-30+1598T>C)
n.350+1598T>C
19g.41352800T>GCA406005291TGFB1,TMEM91c.245A>C (p.Asn82Thr)
c.-30+1598T>G (n.-30+1598T>G)
n.350+1598T>G
19g.41352801T>ACA406005296TGFB1,TMEM91c.244A>T (p.Asn82Tyr)
c.-30+1599T>A (n.-30+1599T>A)
n.350+1599T>A
 dbSNP gnomAD v3 gnomAD v4
19g.41352801T>CCA406005299TGFB1,TMEM91c.244A>G (p.Asn82Asp)
c.-30+1599T>C (n.-30+1599T>C)
n.350+1599T>C
 dbSNP
19g.41352801T>GCA406005298TGFB1,TMEM91c.244A>C (p.Asn82His)
c.-30+1599T>G (n.-30+1599T>G)
n.350+1599T>G
 gnomAD v4
19g.41352801T=CA2336426109TGFB1,TMEM91c.244A= (p.Asn82=)
c.-30+1599T= (n.-30+1599T=)
n.350+1599T=
19g.41352802G>ACA507690091TGFB1,TMEM91c.243C>T (p.Tyr81=)
c.-30+1600G>A (n.-30+1600G>A)
n.350+1600G>A
 gnomAD v4
19g.41352802G>CCA406005301TGFB1,TMEM91c.243C>G (p.Tyr81Ter)
c.-30+1600G>C (n.-30+1600G>C)
n.350+1600G>C
19g.41352802G>TCA406005303TGFB1,TMEM91c.243C>A (p.Tyr81Ter)
c.-30+1600G>T (n.-30+1600G>T)
n.350+1600G>T
19g.41352803T>ACA406005304TGFB1,TMEM91c.242A>T (p.Tyr81Phe)
c.-30+1601T>A (n.-30+1601T>A)
n.350+1601T>A
19g.41352803T>CCA406005309TGFB1,TMEM91c.242A>G (p.Tyr81Cys)
c.-30+1601T>C (n.-30+1601T>C)
n.350+1601T>C
 ClinVar
19g.41352803T>GCA406005305TGFB1,TMEM91c.242A>C (p.Tyr81Ser)
c.-30+1601T>G (n.-30+1601T>G)
n.350+1601T>G
19g.41352804A=CA2336426110TGFB1,TMEM91c.241T= (p.Tyr81=)
c.-30+1602A= (n.-30+1602A=)
n.350+1602A=
19g.41352804A>CCA406005310TGFB1,TMEM91c.241T>G (p.Tyr81Asp)
c.-30+1602A>C (n.-30+1602A>C)
n.350+1602A>C
19g.41352804A>GCA341202TGFB1,TMEM91c.241T>C (p.Tyr81His)
c.-30+1602A>G (n.-30+1602A>G)
n.350+1602A>G
 ClinVar dbSNP gnomAD v4
19g.41352804A>TCA406005314TGFB1,TMEM91c.241T>A (p.Tyr81Asn)
c.-30+1602A>T (n.-30+1602A>T)
n.350+1602A>T
19g.41352805C>ACA507690097TGFB1,TMEM91c.240G>T (p.Leu80=)
c.-30+1603C>A (n.-30+1603C>A)
n.350+1603C>A
 gnomAD v4
19g.41352805C=CA2336426111TGFB1,TMEM91c.240G= (p.Leu80=)
c.-30+1603C= (n.-30+1603C=)
n.350+1603C=
19g.41352805C>GCA507690098TGFB1,TMEM91c.240G>C (p.Leu80=)
c.-30+1603C>G (n.-30+1603C>G)
n.350+1603C>G
19g.41352805C>TCA9460159TGFB1,TMEM91c.240G>A (p.Leu80=)
c.-30+1603C>T (n.-30+1603C>T)
n.350+1603C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352806A>CCA406005321TGFB1,TMEM91c.239T>G (p.Leu80Arg)
c.-30+1604A>C (n.-30+1604A>C)
n.350+1604A>C
19g.41352806A>GCA406005323TGFB1,TMEM91c.239T>C (p.Leu80Pro)
c.-30+1604A>G (n.-30+1604A>G)
n.350+1604A>G
19g.41352806A>TCA406005324TGFB1,TMEM91c.239T>A (p.Leu80Gln)
c.-30+1604A>T (n.-30+1604A>T)
n.350+1604A>T
19g.41352807G>ACA507690100TGFB1,TMEM91c.238C>T (p.Leu80=)
c.-30+1605G>A (n.-30+1605G>A)
n.350+1605G>A
 dbSNP
19g.41352807G>CCA406005327TGFB1,TMEM91c.238C>G (p.Leu80Val)
c.-30+1605G>C (n.-30+1605G>C)
n.350+1605G>C
19g.41352807G=CA2336426112TGFB1,TMEM91c.238C= (p.Leu80=)
c.-30+1605G= (n.-30+1605G=)
n.350+1605G=
19g.41352807G>TCA406005330TGFB1,TMEM91c.238C>A (p.Leu80Met)
c.-30+1605G>T (n.-30+1605G>T)
n.350+1605G>T
19g.41352808G>ACA507690103TGFB1,TMEM91c.237C>T (p.Ala79=)
c.-30+1606G>A (n.-30+1606G>A)
n.350+1606G>A
 dbSNP
19g.41352808G>CCA507690105TGFB1,TMEM91c.237C>G (p.Ala79=)
c.-30+1606G>C (n.-30+1606G>C)
n.350+1606G>C
19g.41352808G=CA2336426113TGFB1,TMEM91c.237C= (p.Ala79=)
c.-30+1606G= (n.-30+1606G=)
n.350+1606G=
19g.41352808G>TCA507690104TGFB1,TMEM91c.237C>A (p.Ala79=)
c.-30+1606G>T (n.-30+1606G>T)
n.350+1606G>T
19g.41352809G>ACA406005334TGFB1,TMEM91c.236C>T (p.Ala79Val)
c.-30+1607G>A (n.-30+1607G>A)
n.350+1607G>A
19g.41352809G>CCA406005343TGFB1,TMEM91c.236C>G (p.Ala79Gly)
c.-30+1607G>C (n.-30+1607G>C)
n.350+1607G>C
19g.41352809G=CA2336426114TGFB1,TMEM91c.236C= (p.Ala79=)
c.-30+1607G= (n.-30+1607G=)
n.350+1607G=
19g.41352809G>TCA406005344TGFB1,TMEM91c.236C>A (p.Ala79Asp)
c.-30+1607G>T (n.-30+1607G>T)
n.350+1607G>T
 dbSNP gnomAD v4
19g.41352810C>ACA406005353TGFB1,TMEM91c.235G>T (p.Ala79Ser)
c.-30+1608C>A (n.-30+1608C>A)
n.350+1608C>A
 dbSNP gnomAD v4
19g.41352810C=CA2336426115TGFB1,TMEM91c.235G= (p.Ala79=)
c.-30+1608C= (n.-30+1608C=)
n.350+1608C=
19g.41352810C>GCA406005348TGFB1,TMEM91c.235G>C (p.Ala79Pro)
c.-30+1608C>G (n.-30+1608C>G)
n.350+1608C>G
19g.41352810C>TCA406005350TGFB1,TMEM91c.235G>A (p.Ala79Thr)
c.-30+1608C>T (n.-30+1608C>T)
n.350+1608C>T
 gnomAD v4
19g.41352811G>ACA507690106TGFB1,TMEM91c.234C>T (p.Leu78=)
c.-30+1609G>A (n.-30+1609G>A)
n.350+1609G>A
19g.41352811G>CCA507690107TGFB1,TMEM91c.234C>G (p.Leu78=)
c.-30+1609G>C (n.-30+1609G>C)
n.350+1609G>C
 gnomAD v4
19g.41352811G>TCA507690108TGFB1,TMEM91c.234C>A (p.Leu78=)
c.-30+1609G>T (n.-30+1609G>T)
n.350+1609G>T
19g.41352812A>CCA406005356TGFB1,TMEM91c.233T>G (p.Leu78Arg)
c.-30+1610A>C (n.-30+1610A>C)
n.350+1610A>C
19g.41352812A>GCA406005357TGFB1,TMEM91c.233T>C (p.Leu78Pro)
c.-30+1610A>G (n.-30+1610A>G)
n.350+1610A>G
19g.41352812A>TCA406005360TGFB1,TMEM91c.233T>A (p.Leu78His)
c.-30+1610A>T (n.-30+1610A>T)
n.350+1610A>T
19g.41352813G>ACA406005366TGFB1,TMEM91c.232C>T (p.Leu78Phe)
c.-30+1611G>A (n.-30+1611G>A)
n.350+1611G>A
 COSMIC
19g.41352813G>CCA406005368TGFB1,TMEM91c.232C>G (p.Leu78Val)
c.-30+1611G>C (n.-30+1611G>C)
n.350+1611G>C
19g.41352813G=CA2336426116TGFB1,TMEM91c.232C= (p.Leu78=)
c.-30+1611G= (n.-30+1611G=)
n.350+1611G=
19g.41352813G>TCA406005370TGFB1,TMEM91c.232C>A (p.Leu78Ile)
c.-30+1611G>T (n.-30+1611G>T)
n.350+1611G>T
 dbSNP gnomAD v3 gnomAD v4
19g.41352814C>ACA507690109TGFB1,TMEM91c.231G>T (p.Val77=)
c.-30+1612C>A (n.-30+1612C>A)
n.350+1612C>A
19g.41352814C=CA2336426117TGFB1,TMEM91c.231G= (p.Val77=)
c.-30+1612C= (n.-30+1612C=)
n.350+1612C=
19g.41352814C>GCA507690110TGFB1,TMEM91c.231G>C (p.Val77=)
c.-30+1612C>G (n.-30+1612C>G)
n.350+1612C>G
 ClinVar dbSNP gnomAD v4
19g.41352814C>TCA507690111TGFB1,TMEM91c.231G>A (p.Val77=)
c.-30+1612C>T (n.-30+1612C>T)
n.350+1612C>T
 gnomAD v4
19g.41352815A>CCA406005375TGFB1,TMEM91c.230T>G (p.Val77Gly)
c.-30+1613A>C (n.-30+1613A>C)
n.350+1613A>C
19g.41352815A>GCA406005377TGFB1,TMEM91c.230T>C (p.Val77Ala)
c.-30+1613A>G (n.-30+1613A>G)
n.350+1613A>G
19g.41352815A>TCA406005379TGFB1,TMEM91c.230T>A (p.Val77Glu)
c.-30+1613A>T (n.-30+1613A>T)
n.350+1613A>T
19g.41352816C>ACA406005382TGFB1,TMEM91c.229G>T (p.Val77Leu)
c.-30+1614C>A (n.-30+1614C>A)
n.350+1614C>A
19g.41352816C=CA2336426118TGFB1,TMEM91c.229G= (p.Val77=)
c.-30+1614C= (n.-30+1614C=)
n.350+1614C=
19g.41352816C>GCA406005386TGFB1,TMEM91c.229G>C (p.Val77Leu)
c.-30+1614C>G (n.-30+1614C>G)
n.350+1614C>G
19g.41352816C>TCA406005389TGFB1,TMEM91c.229G>A (p.Val77Met)
c.-30+1614C>T (n.-30+1614C>T)
n.350+1614C>T
 dbSNP gnomAD v2 gnomAD v4
19g.41352817G>ACA9460160TGFB1,TMEM91c.228C>T (p.Ala76=)
c.-30+1615G>A (n.-30+1615G>A)
n.350+1615G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352817G>CCA308518530TGFB1,TMEM91c.228C>G (p.Ala76=)
c.-30+1615G>C (n.-30+1615G>C)
n.350+1615G>C
 dbSNP
19g.41352817G=CA2336426119TGFB1,TMEM91c.228C= (p.Ala76=)
c.-30+1615G= (n.-30+1615G=)
n.350+1615G=
19g.41352817G>TCA507690113TGFB1,TMEM91c.228C>A (p.Ala76=)
c.-30+1615G>T (n.-30+1615G>T)
n.350+1615G>T
19g.41352818G>ACA406005406TGFB1,TMEM91c.227C>T (p.Ala76Val)
c.-30+1616G>A (n.-30+1616G>A)
n.350+1616G>A
19g.41352818G>CCA406005395TGFB1,TMEM91c.227C>G (p.Ala76Gly)
c.-30+1616G>C (n.-30+1616G>C)
n.350+1616G>C
19g.41352818G>TCA406005398TGFB1,TMEM91c.227C>A (p.Ala76Asp)
c.-30+1616G>T (n.-30+1616G>T)
n.350+1616G>T
19g.41352819C>ACA406005409TGFB1,TMEM91c.226G>T (p.Ala76Ser)
c.-30+1617C>A (n.-30+1617C>A)
n.350+1617C>A
19g.41352819C>GCA406005413TGFB1,TMEM91c.226G>C (p.Ala76Pro)
c.-30+1617C>G (n.-30+1617C>G)
n.350+1617C>G
19g.41352819C>TCA406005417TGFB1,TMEM91c.226G>A (p.Ala76Thr)
c.-30+1617C>T (n.-30+1617C>T)
n.350+1617C>T
 gnomAD v4
19g.41352820C>ACA406005419TGFB1,TMEM91c.225G>T (p.Glu75Asp)
c.-30+1618C>A (n.-30+1618C>A)
n.350+1618C>A
19g.41352820C>GCA406005423TGFB1,TMEM91c.225G>C (p.Glu75Asp)
c.-30+1618C>G (n.-30+1618C>G)
n.350+1618C>G
19g.41352820C>TCA507690118TGFB1,TMEM91c.225G>A (p.Glu75=)
c.-30+1618C>T (n.-30+1618C>T)
n.350+1618C>T
19g.41352821T>ACA406005428TGFB1,TMEM91c.224A>T (p.Glu75Val)
c.-30+1619T>A (n.-30+1619T>A)
n.350+1619T>A
19g.41352821T>CCA406005431TGFB1,TMEM91c.224A>G (p.Glu75Gly)
c.-30+1619T>C (n.-30+1619T>C)
n.350+1619T>C
19g.41352821T>GCA406005430TGFB1,TMEM91c.224A>C (p.Glu75Ala)
c.-30+1619T>G (n.-30+1619T>G)
n.350+1619T>G
19g.41352822C>ACA406005432TGFB1,TMEM91c.223G>T (p.Glu75Ter)
c.-30+1620C>A (n.-30+1620C>A)
n.350+1620C>A
19g.41352822C>GCA406005434TGFB1,TMEM91c.223G>C (p.Glu75Gln)
c.-30+1620C>G (n.-30+1620C>G)
n.350+1620C>G
19g.41352822C>TCA406005443TGFB1,TMEM91c.223G>A (p.Glu75Lys)
c.-30+1620C>T (n.-30+1620C>T)
n.350+1620C>T
 gnomAD v4 COSMIC
19g.41352823G>ACA308518535TGFB1,TMEM91c.222C>T (p.Pro74=)
c.-30+1621G>A (n.-30+1621G>A)
n.350+1621G>A
 dbSNP gnomAD v4
19g.41352823G>CCA507690120TGFB1,TMEM91c.222C>G (p.Pro74=)
c.-30+1621G>C (n.-30+1621G>C)
n.350+1621G>C
 dbSNP gnomAD v2 gnomAD v4
19g.41352823G=CA2336426120TGFB1,TMEM91c.222C= (p.Pro74=)
c.-30+1621G= (n.-30+1621G=)
n.350+1621G=
19g.41352823G>TCA507690121TGFB1,TMEM91c.222C>A (p.Pro74=)
c.-30+1621G>T (n.-30+1621G>T)
n.350+1621G>T
19g.41352824G>ACA406005450TGFB1,TMEM91c.221C>T (p.Pro74Leu)
c.-30+1622G>A (n.-30+1622G>A)
n.350+1622G>A
 dbSNP gnomAD v2 gnomAD v4
19g.41352824G>CCA406005469TGFB1,TMEM91c.221C>G (p.Pro74Arg)
c.-30+1622G>C (n.-30+1622G>C)
n.350+1622G>C
19g.41352824G=CA2336426121TGFB1,TMEM91c.221C= (p.Pro74=)
c.-30+1622G= (n.-30+1622G=)
n.350+1622G=
19g.41352824G>TCA406005460TGFB1,TMEM91c.221C>A (p.Pro74His)
c.-30+1622G>T (n.-30+1622G>T)
n.350+1622G>T
19g.41352825G>ACA406005474TGFB1,TMEM91c.220C>T (p.Pro74Ser)
c.-30+1623G>A (n.-30+1623G>A)
n.350+1623G>A
19g.41352825G>CCA406005492TGFB1,TMEM91c.220C>G (p.Pro74Ala)
c.-30+1623G>C (n.-30+1623G>C)
n.350+1623G>C
19g.41352825G>TCA406005494TGFB1,TMEM91c.220C>A (p.Pro74Thr)
c.-30+1623G>T (n.-30+1623G>T)
n.350+1623G>T
19g.41352826C>ACA507690127TGFB1,TMEM91c.219G>T (p.Leu73=)
c.-30+1624C>A (n.-30+1624C>A)
n.350+1624C>A
19g.41352826C>GCA507690129TGFB1,TMEM91c.219G>C (p.Leu73=)
c.-30+1624C>G (n.-30+1624C>G)
n.350+1624C>G
19g.41352826C>TCA507690130TGFB1,TMEM91c.219G>A (p.Leu73=)
c.-30+1624C>T (n.-30+1624C>T)
n.350+1624C>T
19g.41352827A>CCA406005496TGFB1,TMEM91c.218T>G (p.Leu73Arg)
c.-30+1625A>C (n.-30+1625A>C)
n.350+1625A>C
19g.41352827A>GCA406005498TGFB1,TMEM91c.218T>C (p.Leu73Pro)
c.-30+1625A>G (n.-30+1625A>G)
n.350+1625A>G
19g.41352827A>TCA406005501TGFB1,TMEM91c.218T>A (p.Leu73Gln)
c.-30+1625A>T (n.-30+1625A>T)
n.350+1625A>T
19g.41352828G>ACA507690131TGFB1,TMEM91c.217C>T (p.Leu73=)
c.-30+1626G>A (n.-30+1626G>A)
n.350+1626G>A
19g.41352828G>CCA406005511TGFB1,TMEM91c.217C>G (p.Leu73Val)
c.-30+1626G>C (n.-30+1626G>C)
n.350+1626G>C
19g.41352828G>TCA406005514TGFB1,TMEM91c.217C>A (p.Leu73Met)
c.-30+1626G>T (n.-30+1626G>T)
n.350+1626G>T
19g.41352829C>ACA507690132TGFB1,TMEM91c.216G>T (p.Pro72=)
c.-30+1627C>A (n.-30+1627C>A)
n.350+1627C>A
 gnomAD v4
19g.41352829C=CA2336426122TGFB1,TMEM91c.216G= (p.Pro72=)
c.-30+1627C= (n.-30+1627C=)
n.350+1627C=
19g.41352829C>GCA507690133TGFB1,TMEM91c.216G>C (p.Pro72=)
c.-30+1627C>G (n.-30+1627C>G)
n.350+1627C>G
 gnomAD v4
19g.41352829C>TCA308518542TGFB1,TMEM91c.216G>A (p.Pro72=)
c.-30+1627C>T (n.-30+1627C>T)
n.350+1627C>T
 dbSNP gnomAD v2 gnomAD v4
19g.41352830G>ACA406005516TGFB1,TMEM91c.215C>T (p.Pro72Leu)
c.-30+1628G>A (n.-30+1628G>A)
n.350+1628G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41352830G>CCA406005519TGFB1,TMEM91c.215C>G (p.Pro72Arg)
c.-30+1628G>C (n.-30+1628G>C)
n.350+1628G>C
 gnomAD v4
19g.41352830G=CA2336426123TGFB1,TMEM91c.215C= (p.Pro72=)
c.-30+1628G= (n.-30+1628G=)
n.350+1628G=
19g.41352830G>TCA9460161TGFB1,TMEM91c.215C>A (p.Pro72Gln)
c.-30+1628G>T (n.-30+1628G>T)
n.350+1628G>T
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41352831G>ACA406005531TGFB1,TMEM91c.214C>T (p.Pro72Ser)
c.-30+1629G>A (n.-30+1629G>A)
n.350+1629G>A
19g.41352831G>CCA406005528TGFB1,TMEM91c.214C>G (p.Pro72Ala)
c.-30+1629G>C (n.-30+1629G>C)
n.350+1629G>C
19g.41352831G>TCA406005525TGFB1,TMEM91c.214C>A (p.Pro72Thr)
c.-30+1629G>T (n.-30+1629G>T)
n.350+1629G>T
19g.41352832G>ACA507690137TGFB1,TMEM91c.213C>T (p.Gly71=)
c.-30+1630G>A (n.-30+1630G>A)
n.350+1630G>A
 dbSNP gnomAD v2 gnomAD v4
19g.41352832G>CCA507690138TGFB1,TMEM91c.213C>G (p.Gly71=)
c.-30+1630G>C (n.-30+1630G>C)
n.350+1630G>C
19g.41352832G=CA2336426124TGFB1,TMEM91c.213C= (p.Gly71=)
c.-30+1630G= (n.-30+1630G=)
n.350+1630G=
19g.41352832G>TCA507690139TGFB1,TMEM91c.213C>A (p.Gly71=)
c.-30+1630G>T (n.-30+1630G>T)
n.350+1630G>T
 dbSNP
19g.41352833C>ACA406005538TGFB1,TMEM91c.212G>T (p.Gly71Val)
c.-30+1631C>A (n.-30+1631C>A)
n.350+1631C>A
 gnomAD v4
19g.41352833C>GCA406005534TGFB1,TMEM91c.212G>C (p.Gly71Ala)
c.-30+1631C>G (n.-30+1631C>G)
n.350+1631C>G
19g.41352833C>TCA406005540TGFB1,TMEM91c.212G>A (p.Gly71Asp)
c.-30+1631C>T (n.-30+1631C>T)
n.350+1631C>T
 ClinVar gnomAD v4
19g.41352834C>ACA406005543TGFB1,TMEM91c.211G>T (p.Gly71Cys)
c.-30+1632C>A (n.-30+1632C>A)
n.350+1632C>A
19g.41352834C=CA2336426125TGFB1,TMEM91c.211G= (p.Gly71=)
c.-30+1632C= (n.-30+1632C=)
n.350+1632C=
19g.41352834C>GCA406005547TGFB1,TMEM91c.211G>C (p.Gly71Arg)
c.-30+1632C>G (n.-30+1632C>G)
n.350+1632C>G
19g.41352834C>TCA308518577TGFB1,TMEM91c.211G>A (p.Gly71Ser)
c.-30+1632C>T (n.-30+1632C>T)
n.350+1632C>T
 dbSNP gnomAD v4
19g.41352835G>ACA507690143TGFB1,TMEM91c.210C>T (p.Pro70=)
c.-30+1633G>A (n.-30+1633G>A)
n.350+1633G>A
 dbSNP gnomAD v2 gnomAD v4
19g.41352835G>CCA507690145TGFB1,TMEM91c.210C>G (p.Pro70=)
c.-30+1633G>C (n.-30+1633G>C)
n.350+1633G>C
19g.41352835G=CA2336426126TGFB1,TMEM91c.210C= (p.Pro70=)
c.-30+1633G= (n.-30+1633G=)
n.350+1633G=
19g.41352835G>TCA507690146TGFB1,TMEM91c.210C>A (p.Pro70=)
c.-30+1633G>T (n.-30+1633G>T)
n.350+1633G>T
19g.41352836G>ACA406005550TGFB1,TMEM91c.209C>T (p.Pro70Leu)
c.-30+1634G>A (n.-30+1634G>A)
n.350+1634G>A
 dbSNP
19g.41352836G>CCA406005553TGFB1,TMEM91c.209C>G (p.Pro70Arg)
c.-30+1634G>C (n.-30+1634G>C)
n.350+1634G>C
19g.41352836G=CA2336426127TGFB1,TMEM91c.209C= (p.Pro70=)
c.-30+1634G= (n.-30+1634G=)
n.350+1634G=
19g.41352836G>TCA406005557TGFB1,TMEM91c.209C>A (p.Pro70His)
c.-30+1634G>T (n.-30+1634G>T)
n.350+1634G>T
19g.41352837G>ACA406005561TGFB1,TMEM91c.208C>T (p.Pro70Ser)
c.-30+1635G>A (n.-30+1635G>A)
n.350+1635G>A
 gnomAD v4
19g.41352837G>CCA406005564TGFB1,TMEM91c.208C>G (p.Pro70Ala)
c.-30+1635G>C (n.-30+1635G>C)
n.350+1635G>C
19g.41352837G>TCA406005567TGFB1,TMEM91c.208C>A (p.Pro70Thr)
c.-30+1635G>T (n.-30+1635G>T)
n.350+1635G>T
19g.41352838C>ACA507690151TGFB1,TMEM91c.207G>T (p.Pro69=)
c.-30+1636C>A (n.-30+1636C>A)
n.350+1636C>A
 gnomAD v4
19g.41352838C>GCA507690153TGFB1,TMEM91c.207G>C (p.Pro69=)
c.-30+1636C>G (n.-30+1636C>G)
n.350+1636C>G
19g.41352838C>TCA507690152TGFB1,TMEM91c.207G>A (p.Pro69=)
c.-30+1636C>T (n.-30+1636C>T)
n.350+1636C>T
 gnomAD v4
19g.41352839G>ACA9460162TGFB1,TMEM91c.206C>T (p.Pro69Leu)
c.-30+1637G>A (n.-30+1637G>A)
n.350+1637G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352839G>CCA406005570TGFB1,TMEM91c.206C>G (p.Pro69Arg)
c.-30+1637G>C (n.-30+1637G>C)
n.350+1637G>C
19g.41352839G=CA2336426128TGFB1,TMEM91c.206C= (p.Pro69=)
c.-30+1637G= (n.-30+1637G=)
n.350+1637G=
19g.41352839G>TCA406005574TGFB1,TMEM91c.206C>A (p.Pro69Gln)
c.-30+1637G>T (n.-30+1637G>T)
n.350+1637G>T
 gnomAD v4
19g.41352840G>ACA406005581TGFB1,TMEM91c.205C>T (p.Pro69Ser)
c.-30+1638G>A (n.-30+1638G>A)
n.350+1638G>A
 gnomAD v4
19g.41352840G>CCA406005579TGFB1,TMEM91c.205C>G (p.Pro69Ala)
c.-30+1638G>C (n.-30+1638G>C)
n.350+1638G>C
19g.41352840G>TCA406005580TGFB1,TMEM91c.205C>A (p.Pro69Thr)
c.-30+1638G>T (n.-30+1638G>T)
n.350+1638G>T
19g.41352841C>ACA507690157TGFB1,TMEM91c.204G>T (p.Val68=)
c.-30+1639C>A (n.-30+1639C>A)
n.350+1639C>A
 dbSNP gnomAD v2 gnomAD v4
19g.41352841C=CA2336426129TGFB1,TMEM91c.204G= (p.Val68=)
c.-30+1639C= (n.-30+1639C=)
n.350+1639C=
19g.41352841C>GCA507690158TGFB1,TMEM91c.204G>C (p.Val68=)
c.-30+1639C>G (n.-30+1639C>G)
n.350+1639C>G
 gnomAD v4
19g.41352841C>TCA507690159TGFB1,TMEM91c.204G>A (p.Val68=)
c.-30+1639C>T (n.-30+1639C>T)
n.350+1639C>T
 gnomAD v4
19g.41352842_41352844delCA2585297352TGFB1,TMEM91c.202_204del (p.Val68del)
c.-30+1640_-30+1642del (n.-30+1640_-30+1642del)
n.350+1640_350+1642del
 ClinVar gnomAD v4
19g.41352842A=CA2336426130TGFB1,TMEM91c.203T= (p.Val68=)
c.-30+1640A= (n.-30+1640A=)
n.350+1640A=
19g.41352842A>CCA308518579TGFB1,TMEM91c.203T>G (p.Val68Gly)
c.-30+1640A>C (n.-30+1640A>C)
n.350+1640A>C
 dbSNP gnomAD v2 gnomAD v4
19g.41352842A>GCA406005589TGFB1,TMEM91c.203T>C (p.Val68Ala)
c.-30+1640A>G (n.-30+1640A>G)
n.350+1640A>G
 gnomAD v4
19g.41352842A>TCA406005593TGFB1,TMEM91c.203T>A (p.Val68Glu)
c.-30+1640A>T (n.-30+1640A>T)
n.350+1640A>T
19g.41352843C>ACA406005597TGFB1,TMEM91c.202G>T (p.Val68Leu)
c.-30+1641C>A (n.-30+1641C>A)
n.350+1641C>A
 dbSNP gnomAD v4
19g.41352843C=CA2336426131TGFB1,TMEM91c.202G= (p.Val68=)
c.-30+1641C= (n.-30+1641C=)
n.350+1641C=
19g.41352843C>GCA406005599TGFB1,TMEM91c.202G>C (p.Val68Leu)
c.-30+1641C>G (n.-30+1641C>G)
n.350+1641C>G
19g.41352843C>TCA406005602TGFB1,TMEM91c.202G>A (p.Val68Met)
c.-30+1641C>T (n.-30+1641C>T)
n.350+1641C>T
19g.41352844C>ACA406005606TGFB1,TMEM91c.201G>T (p.Glu67Asp)
c.-30+1642C>A (n.-30+1642C>A)
n.350+1642C>A
19g.41352844C=CA2336426132TGFB1,TMEM91c.201G= (p.Glu67=)
c.-30+1642C= (n.-30+1642C=)
n.350+1642C=
19g.41352844C>GCA406005608TGFB1,TMEM91c.201G>C (p.Glu67Asp)
c.-30+1642C>G (n.-30+1642C>G)
n.350+1642C>G
19g.41352844C>TCA507690160TGFB1,TMEM91c.201G>A (p.Glu67=)
c.-30+1642C>T (n.-30+1642C>T)
n.350+1642C>T
 dbSNP gnomAD v3 gnomAD v4
19g.41352845T>ACA406005612TGFB1,TMEM91c.200A>T (p.Glu67Val)
c.-30+1643T>A (n.-30+1643T>A)
n.350+1643T>A
19g.41352845T>CCA406005615TGFB1,TMEM91c.200A>G (p.Glu67Gly)
c.-30+1643T>C (n.-30+1643T>C)
n.350+1643T>C
 gnomAD v4 COSMIC
19g.41352845T>GCA406005619TGFB1,TMEM91c.200A>C (p.Glu67Ala)
c.-30+1643T>G (n.-30+1643T>G)
n.350+1643T>G
19g.41352846C>ACA406005625TGFB1,TMEM91c.199G>T (p.Glu67Ter)
c.-30+1644C>A (n.-30+1644C>A)
n.350+1644C>A
19g.41352846C>GCA406005628TGFB1,TMEM91c.199G>C (p.Glu67Gln)
c.-30+1644C>G (n.-30+1644C>G)
n.350+1644C>G
19g.41352846C>TCA406005623TGFB1,TMEM91c.199G>A (p.Glu67Lys)
c.-30+1644C>T (n.-30+1644C>T)
n.350+1644C>T
 gnomAD v4
19g.41352847C>ACA507690161TGFB1,TMEM91c.198G>T (p.Gly66=)
c.-30+1645C>A (n.-30+1645C>A)
n.350+1645C>A
19g.41352847C=CA2336426133TGFB1,TMEM91c.198G= (p.Gly66=)
c.-30+1645C= (n.-30+1645C=)
n.350+1645C=
19g.41352847C>GCA507690162TGFB1,TMEM91c.198G>C (p.Gly66=)
c.-30+1645C>G (n.-30+1645C>G)
n.350+1645C>G
 dbSNP gnomAD v3 gnomAD v4
19g.41352847C>TCA9460163TGFB1,TMEM91c.198G>A (p.Gly66=)
c.-30+1645C>T (n.-30+1645C>T)
n.350+1645C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352848C>ACA406005634TGFB1,TMEM91c.197G>T (p.Gly66Val)
c.-30+1646C>A (n.-30+1646C>A)
n.350+1646C>A
19g.41352848C>GCA406005636TGFB1,TMEM91c.197G>C (p.Gly66Ala)
c.-30+1646C>G (n.-30+1646C>G)
n.350+1646C>G
 gnomAD v4
19g.41352848C>TCA406005638TGFB1,TMEM91c.197G>A (p.Gly66Glu)
c.-30+1646C>T (n.-30+1646C>T)
n.350+1646C>T
19g.41352849C>ACA406005644TGFB1,TMEM91c.196G>T (p.Gly66Trp)
c.-30+1647C>A (n.-30+1647C>A)
n.350+1647C>A
19g.41352849C>GCA406005649TGFB1,TMEM91c.196G>C (p.Gly66Arg)
c.-30+1647C>G (n.-30+1647C>G)
n.350+1647C>G
19g.41352849C>TCA406005651TGFB1,TMEM91c.196G>A (p.Gly66Arg)
c.-30+1647C>T (n.-30+1647C>T)
n.350+1647C>T
19g.41352850C>ACA406005662TGFB1,TMEM91c.195G>T (p.Gln65His)
c.-30+1648C>A (n.-30+1648C>A)
n.350+1648C>A
 gnomAD v4
19g.41352850C>GCA406005664TGFB1,TMEM91c.195G>C (p.Gln65His)
c.-30+1648C>G (n.-30+1648C>G)
n.350+1648C>G
19g.41352850C>TCA507690163TGFB1,TMEM91c.195G>A (p.Gln65=)
c.-30+1648C>T (n.-30+1648C>T)
n.350+1648C>T
19g.41352851T>ACA406005667TGFB1,TMEM91c.194A>T (p.Gln65Leu)
c.-30+1649T>A (n.-30+1649T>A)
n.350+1649T>A
19g.41352851T>CCA406005669TGFB1,TMEM91c.194A>G (p.Gln65Arg)
c.-30+1649T>C (n.-30+1649T>C)
n.350+1649T>C
 gnomAD v4
19g.41352851T>GCA406005673TGFB1,TMEM91c.194A>C (p.Gln65Pro)
c.-30+1649T>G (n.-30+1649T>G)
n.350+1649T>G
 gnomAD v4
19g.41352852G>ACA406005678TGFB1,TMEM91c.193C>T (p.Gln65Ter)
c.-30+1650G>A (n.-30+1650G>A)
n.350+1650G>A
 ClinVar gnomAD v4
19g.41352852G>CCA406005681TGFB1,TMEM91c.193C>G (p.Gln65Glu)
c.-30+1650G>C (n.-30+1650G>C)
n.350+1650G>C
19g.41352852G>TCA406005677TGFB1,TMEM91c.193C>A (p.Gln65Lys)
c.-30+1650G>T (n.-30+1650G>T)
n.350+1650G>T
19g.41352853G>ACA507690164TGFB1,TMEM91c.192C>T (p.Ser64=)
c.-30+1651G>A (n.-30+1651G>A)
n.350+1651G>A
 gnomAD v4
19g.41352853G>CCA406005685TGFB1,TMEM91c.192C>G (p.Ser64Arg)
c.-30+1651G>C (n.-30+1651G>C)
n.350+1651G>C
19g.41352853G>TCA406005688TGFB1,TMEM91c.192C>A (p.Ser64Arg)
c.-30+1651G>T (n.-30+1651G>T)
n.350+1651G>T
19g.41352854C>ACA406005692TGFB1,TMEM91c.191G>T (p.Ser64Ile)
c.-30+1652C>A (n.-30+1652C>A)
n.350+1652C>A
 gnomAD v4
19g.41352854C=CA2336426134TGFB1,TMEM91c.191G= (p.Ser64=)
c.-30+1652C= (n.-30+1652C=)
n.350+1652C=
19g.41352854C>GCA9460164TGFB1,TMEM91c.191G>C (p.Ser64Thr)
c.-30+1652C>G (n.-30+1652C>G)
n.350+1652C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352854C>TCA406005697TGFB1,TMEM91c.191G>A (p.Ser64Asn)
c.-30+1652C>T (n.-30+1652C>T)
n.350+1652C>T
19g.41352855T>ACA406005713TGFB1,TMEM91c.190A>T (p.Ser64Cys)
c.-30+1653T>A (n.-30+1653T>A)
n.350+1653T>A
19g.41352855T>CCA406005704TGFB1,TMEM91c.190A>G (p.Ser64Gly)
c.-30+1653T>C (n.-30+1653T>C)
n.350+1653T>C
19g.41352855T>GCA406005701TGFB1,TMEM91c.190A>C (p.Ser64Arg)
c.-30+1653T>G (n.-30+1653T>G)
n.350+1653T>G
19g.41352855_41352856delinsTCCA2336426135TGFB1,TMEM91c.189_190delinsGA (p.Pro63=)
c.-30+1653_-30+1654delinsTC (n.-30+1653_-30+1654delinsTC)
n.350+1653_350+1654delinsTC
19g.41352856delCA9460165TGFB1,TMEM91c.189del (p.Ser64AlafsTer?)
c.-30+1654del (n.-30+1654del)
n.350+1654del
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41352856C>ACA507690165TGFB1,TMEM91c.189G>T (p.Pro63=)
c.-30+1654C>A (n.-30+1654C>A)
n.350+1654C>A
 gnomAD v4
19g.41352856C=CA2336426137TGFB1,TMEM91c.189G= (p.Pro63=)
c.-30+1654C= (n.-30+1654C=)
n.350+1654C=
19g.41352856C>GCA308518590TGFB1,TMEM91c.189G>C (p.Pro63=)
c.-30+1654C>G (n.-30+1654C>G)
n.350+1654C>G
 dbSNP gnomAD v4
19g.41352856C>TCA507690166TGFB1,TMEM91c.189G>A (p.Pro63=)
c.-30+1654C>T (n.-30+1654C>T)
n.350+1654C>T
 dbSNP gnomAD v2 gnomAD v4
19g.41352856_41352857delinsCGCA2336426136TGFB1,TMEM91c.188_189delinsCG (p.Pro63=)
c.-30+1654_-30+1655delinsCG (n.-30+1654_-30+1655delinsCG)
n.350+1654_350+1655delinsCG
19g.41352857G>ACA406005719TGFB1,TMEM91c.188C>T (p.Pro63Leu)
c.-30+1655G>A (n.-30+1655G>A)
n.350+1655G>A
 gnomAD v4
19g.41352857G>CCA406005722TGFB1,TMEM91c.188C>G (p.Pro63Arg)
c.-30+1655G>C (n.-30+1655G>C)
n.350+1655G>C
19g.41352857G>TCA406005725TGFB1,TMEM91c.188C>A (p.Pro63Gln)
c.-30+1655G>T (n.-30+1655G>T)
n.350+1655G>T
 dbSNP
19g.41352862dupCA633470196TGFB1,TMEM91c.188dup (p.Ser64GlufsTer?)
c.-30+1660dup (n.-30+1660dup)
n.350+1660dup
 gnomAD v2 gnomAD v4
19g.41352862delCA2336426138TGFB1,TMEM91c.188del (p.Pro63ArgfsTer?)
c.-30+1660del (n.-30+1660del)
n.350+1660del
 dbSNP gnomAD v4
19g.41352858G>ACA406005730TGFB1,TMEM91c.187C>T (p.Pro63Ser)
c.-30+1656G>A (n.-30+1656G>A)
n.350+1656G>A
19g.41352858G>CCA406005732TGFB1,TMEM91c.187C>G (p.Pro63Ala)
c.-30+1656G>C (n.-30+1656G>C)
n.350+1656G>C
19g.41352858G>TCA406005735TGFB1,TMEM91c.187C>A (p.Pro63Thr)
c.-30+1656G>T (n.-30+1656G>T)
n.350+1656G>T
19g.41352859G>ACA507690167TGFB1,TMEM91c.186C>T (p.Pro62=)
c.-30+1657G>A (n.-30+1657G>A)
n.350+1657G>A
19g.41352859G>CCA507690168TGFB1,TMEM91c.186C>G (p.Pro62=)
c.-30+1657G>C (n.-30+1657G>C)
n.350+1657G>C
 gnomAD v4
19g.41352859G>TCA507690169TGFB1,TMEM91c.186C>A (p.Pro62=)
c.-30+1657G>T (n.-30+1657G>T)
n.350+1657G>T
19g.41352860G>ACA406005740TGFB1,TMEM91c.185C>T (p.Pro62Leu)
c.-30+1658G>A (n.-30+1658G>A)
n.350+1658G>A
 dbSNP gnomAD v3 gnomAD v4
19g.41352860G>CCA406005743TGFB1,TMEM91c.185C>G (p.Pro62Arg)
c.-30+1658G>C (n.-30+1658G>C)
n.350+1658G>C
19g.41352860G=CA2336426139TGFB1,TMEM91c.185C= (p.Pro62=)
c.-30+1658G= (n.-30+1658G=)
n.350+1658G=
19g.41352860G>TCA406005738TGFB1,TMEM91c.185C>A (p.Pro62His)
c.-30+1658G>T (n.-30+1658G>T)
n.350+1658G>T
 gnomAD v4
19g.41352861G>ACA406005746TGFB1,TMEM91c.184C>T (p.Pro62Ser)
c.-30+1659G>A (n.-30+1659G>A)
n.350+1659G>A
19g.41352861G>CCA406005753TGFB1,TMEM91c.184C>G (p.Pro62Ala)
c.-30+1659G>C (n.-30+1659G>C)
n.350+1659G>C
19g.41352861G>TCA406005751TGFB1,TMEM91c.184C>A (p.Pro62Thr)
c.-30+1659G>T (n.-30+1659G>T)
n.350+1659G>T
 ClinVar
19g.41352862G>ACA507690170TGFB1,TMEM91c.183C>T (p.Ser61=)
c.-30+1660G>A (n.-30+1660G>A)
n.350+1660G>A
19g.41352862G>CCA406005755TGFB1,TMEM91c.183C>G (p.Ser61Arg)
c.-30+1660G>C (n.-30+1660G>C)
n.350+1660G>C
19g.41352862G>TCA406005758TGFB1,TMEM91c.183C>A (p.Ser61Arg)
c.-30+1660G>T (n.-30+1660G>T)
n.350+1660G>T
 ClinVar dbSNP gnomAD v4
19g.41352862_41352867delinsGCTGGCCA2336426140TGFB1,TMEM91c.178_183delinsGCCAGC (p.Ala60=)
c.-30+1660_-30+1665delinsGCTGGC (n.-30+1660_-30+1665delinsGCTGGC)
n.350+1660_350+1665delinsGCTGGC
19g.41352863C>ACA406005764TGFB1,TMEM91c.182G>T (p.Ser61Ile)
c.-30+1661C>A (n.-30+1661C>A)
n.350+1661C>A
 gnomAD v4
19g.41352863C>GCA406005766TGFB1,TMEM91c.182G>C (p.Ser61Thr)
c.-30+1661C>G (n.-30+1661C>G)
n.350+1661C>G
 gnomAD v4
19g.41352863C>TCA406005775TGFB1,TMEM91c.182G>A (p.Ser61Asn)
c.-30+1661C>T (n.-30+1661C>T)
n.350+1661C>T
 gnomAD v4
19g.41352863_41352867delCA507690171TGFB1,TMEM91c.178_182del (p.Ala60ProfsTer?)
c.-30+1661_-30+1665del (n.-30+1661_-30+1665del)
n.350+1661_350+1665del
 dbSNP
19g.41352864T>ACA406005778TGFB1,TMEM91c.181A>T (p.Ser61Cys)
c.-30+1662T>A (n.-30+1662T>A)
n.350+1662T>A
19g.41352864T>CCA406005780TGFB1,TMEM91c.181A>G (p.Ser61Gly)
c.-30+1662T>C (n.-30+1662T>C)
n.350+1662T>C
 dbSNP gnomAD v3 gnomAD v4
19g.41352864T>GCA308518599TGFB1,TMEM91c.181A>C (p.Ser61Arg)
c.-30+1662T>G (n.-30+1662T>G)
n.350+1662T>G
 dbSNP gnomAD v2 gnomAD v4
19g.41352864T=CA2336426141TGFB1,TMEM91c.181A= (p.Ser61=)
c.-30+1662T= (n.-30+1662T=)
n.350+1662T=
19g.41352864_41352868delCA406005787TGFB1,TMEM91c.177_181del (p.Ala60ProfsTer?)
c.-30+1662_-30+1666del (n.-30+1662_-30+1666del)
n.350+1662_350+1666del
19g.41352865G>ACA507690174TGFB1,TMEM91c.180C>T (p.Ala60=)
c.-30+1663G>A (n.-30+1663G>A)
n.350+1663G>A
 gnomAD v4
19g.41352865G>CCA507690172TGFB1,TMEM91c.180C>G (p.Ala60=)
c.-30+1663G>C (n.-30+1663G>C)
n.350+1663G>C
19g.41352865G>TCA507690173TGFB1,TMEM91c.180C>A (p.Ala60=)
c.-30+1663G>T (n.-30+1663G>T)
n.350+1663G>T
19g.41352866G>ACA406005791TGFB1,TMEM91c.179C>T (p.Ala60Val)
c.-30+1664G>A (n.-30+1664G>A)
n.350+1664G>A
 gnomAD v4
19g.41352866G>CCA406005792TGFB1,TMEM91c.179C>G (p.Ala60Gly)
c.-30+1664G>C (n.-30+1664G>C)
n.350+1664G>C
 ClinVar
19g.41352866G>TCA406005796TGFB1,TMEM91c.179C>A (p.Ala60Asp)
c.-30+1664G>T (n.-30+1664G>T)
n.350+1664G>T
 gnomAD v4
19g.41352867C>ACA406005799TGFB1,TMEM91c.178G>T (p.Ala60Ser)
c.-30+1665C>A (n.-30+1665C>A)
n.350+1665C>A
 gnomAD v4
19g.41352867C=CA2336426142TGFB1,TMEM91c.178G= (p.Ala60=)
c.-30+1665C= (n.-30+1665C=)
n.350+1665C=
19g.41352867C>GCA9460166TGFB1,TMEM91c.178G>C (p.Ala60Pro)
c.-30+1665C>G (n.-30+1665C>G)
n.350+1665C>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41352867C>TCA406005803TGFB1,TMEM91c.178G>A (p.Ala60Thr)
c.-30+1665C>T (n.-30+1665C>T)
n.350+1665C>T
 gnomAD v4
19g.41352868G>ACA507690175TGFB1,TMEM91c.177C>T (p.Leu59=)
c.-30+1666G>A (n.-30+1666G>A)
n.350+1666G>A
 gnomAD v4
19g.41352868G>CCA507690176TGFB1,TMEM91c.177C>G (p.Leu59=)
c.-30+1666G>C (n.-30+1666G>C)
n.350+1666G>C
19g.41352868G>TCA507690177TGFB1,TMEM91c.177C>A (p.Leu59=)
c.-30+1666G>T (n.-30+1666G>T)
n.350+1666G>T
 gnomAD v4
19g.41352869A>CCA406005806TGFB1,TMEM91c.176T>G (p.Leu59Arg)
c.-30+1667A>C (n.-30+1667A>C)
n.350+1667A>C
19g.41352869A>GCA406005808TGFB1,TMEM91c.176T>C (p.Leu59Pro)
c.-30+1667A>G (n.-30+1667A>G)
n.350+1667A>G
19g.41352869A>TCA406005807TGFB1,TMEM91c.176T>A (p.Leu59His)
c.-30+1667A>T (n.-30+1667A>T)
n.350+1667A>T
19g.41352870G>ACA406005811TGFB1,TMEM91c.175C>T (p.Leu59Phe)
c.-30+1668G>A (n.-30+1668G>A)
n.350+1668G>A
 gnomAD v4
19g.41352870G>CCA406005813TGFB1,TMEM91c.175C>G (p.Leu59Val)
c.-30+1668G>C (n.-30+1668G>C)
n.350+1668G>C
19g.41352870G=CA2336426143TGFB1,TMEM91c.175C= (p.Leu59=)
c.-30+1668G= (n.-30+1668G=)
n.350+1668G=
19g.41352870G>TCA308518616TGFB1,TMEM91c.175C>A (p.Leu59Ile)
c.-30+1668G>T (n.-30+1668G>T)
n.350+1668G>T
 dbSNP

Number of alleles fetched