Chr Mutation (hg38) CAid Gene Transcript Linkouts
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.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
19g.41352992A>CCA406006389TGFB1,TMEM91c.53T>G (p.Leu18Arg)
c.-30+1790A>C (n.-30+1790A>C)
n.350+1790A>C
19g.41352992A>GCA406006391TGFB1,TMEM91c.53T>C (p.Leu18Pro)
c.-30+1790A>G (n.-30+1790A>G)
n.350+1790A>G
 gnomAD v4
19g.41352992A>TCA406006390TGFB1,TMEM91c.53T>A (p.Leu18Gln)
c.-30+1790A>T (n.-30+1790A>T)
n.350+1790A>T
19g.41352993G>ACA507690425TGFB1,TMEM91c.52C>T (p.Leu18=)
c.-30+1791G>A (n.-30+1791G>A)
n.350+1791G>A
 ClinVar dbSNP gnomAD v4
19g.41352993G>CCA406006393TGFB1,TMEM91c.52C>G (p.Leu18Val)
c.-30+1791G>C (n.-30+1791G>C)
n.350+1791G>C
19g.41352993G=CA2336426204TGFB1,TMEM91c.52C= (p.Leu18=)
c.-30+1791G= (n.-30+1791G=)
n.350+1791G=
19g.41352993G>TCA406006394TGFB1,TMEM91c.52C>A (p.Leu18Ile)
c.-30+1791G>T (n.-30+1791G>T)
n.350+1791G>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41352994C>ACA406006395TGFB1,TMEM91c.51G>T (p.Trp17Cys)
c.-30+1792C>A (n.-30+1792C>A)
n.350+1792C>A
 gnomAD v4
19g.41352994C>GCA406006396TGFB1,TMEM91c.51G>C (p.Trp17Cys)
c.-30+1792C>G (n.-30+1792C>G)
n.350+1792C>G
 gnomAD v4

Number of alleles fetched