Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
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
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
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

Number of alleles fetched