Chr Mutation (hg38) CAid Gene Transcript Linkouts
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

Number of alleles fetched