Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.41352877C>A | CA406005846 | TGFB1,TMEM91 | c.168G>T (p.Lys56Asn) c.-30+1675C>A (n.-30+1675C>A) n.350+1675C>A | gnomAD v4 |
19 | g.41352877C>G | CA406005848 | TGFB1,TMEM91 | c.168G>C (p.Lys56Asn) c.-30+1675C>G (n.-30+1675C>G) n.350+1675C>G | |
19 | g.41352877C>T | CA507690186 | TGFB1,TMEM91 | c.168G>A (p.Lys56=) c.-30+1675C>T (n.-30+1675C>T) n.350+1675C>T | gnomAD v4 |
19 | g.41352878T>A | CA406005851 | TGFB1,TMEM91 | c.167A>T (p.Lys56Met) c.-30+1676T>A (n.-30+1676T>A) n.350+1676T>A | |
19 | g.41352878T>C | CA406005854 | TGFB1,TMEM91 | c.167A>G (p.Lys56Arg) c.-30+1676T>C (n.-30+1676T>C) n.350+1676T>C | |
19 | g.41352878T>G | CA406005857 | TGFB1,TMEM91 | c.167A>C (p.Lys56Thr) c.-30+1676T>G (n.-30+1676T>G) n.350+1676T>G | gnomAD v4 |
19 | g.41352879T>A | CA406005860 | TGFB1,TMEM91 | c.166A>T (p.Lys56Ter) c.-30+1677T>A (n.-30+1677T>A) n.350+1677T>A | |
19 | g.41352879T>C | CA406005862 | TGFB1,TMEM91 | c.166A>G (p.Lys56Glu) c.-30+1677T>C (n.-30+1677T>C) n.350+1677T>C | |
19 | g.41352879T>G | CA406005865 | TGFB1,TMEM91 | c.166A>C (p.Lys56Gln) c.-30+1677T>G (n.-30+1677T>G) n.350+1677T>G | |
19 | g.41352880G>A | CA507690189 | TGFB1,TMEM91 | c.165C>T (p.Ser55=) c.-30+1678G>A (n.-30+1678G>A) n.350+1678G>A | gnomAD v4 |
19 | g.41352880G>C | CA507690188 | TGFB1,TMEM91 | c.165C>G (p.Ser55=) c.-30+1678G>C (n.-30+1678G>C) n.350+1678G>C | gnomAD v4 |
19 | g.41352880G>T | CA507690187 | TGFB1,TMEM91 | c.165C>A (p.Ser55=) c.-30+1678G>T (n.-30+1678G>T) n.350+1678G>T | gnomAD v4 |
19 | g.41352881G>A | CA406005869 | TGFB1,TMEM91 | c.164C>T (p.Ser55Phe) c.-30+1679G>A (n.-30+1679G>A) n.350+1679G>A | |
19 | g.41352881G>C | CA406005871 | TGFB1,TMEM91 | c.164C>G (p.Ser55Cys) c.-30+1679G>C (n.-30+1679G>C) n.350+1679G>C | gnomAD v4 |
19 | g.41352881G>T | CA406005875 | TGFB1,TMEM91 | c.164C>A (p.Ser55Tyr) c.-30+1679G>T (n.-30+1679G>T) n.350+1679G>T | gnomAD v4 |
19 | g.41352882A= | CA2336426146 | TGFB1,TMEM91 | c.163T= (p.Ser55=) c.-30+1680A= (n.-30+1680A=) n.350+1680A= | |
19 | g.41352882A>C | CA406005882 | TGFB1,TMEM91 | c.163T>G (p.Ser55Ala) c.-30+1680A>C (n.-30+1680A>C) n.350+1680A>C | |
19 | g.41352882A>G | CA308518620 | TGFB1,TMEM91 | c.163T>C (p.Ser55Pro) c.-30+1680A>G (n.-30+1680A>G) n.350+1680A>G | dbSNP |
19 | g.41352882A>T | CA406005879 | TGFB1,TMEM91 | c.163T>A (p.Ser55Thr) c.-30+1680A>T (n.-30+1680A>T) n.350+1680A>T | |
19 | g.41352883C>A | CA507690190 | TGFB1,TMEM91 | c.162G>T (p.Leu54=) c.-30+1681C>A (n.-30+1681C>A) n.350+1681C>A | |
19 | g.41352883C= | CA2336426147 | TGFB1,TMEM91 | c.162G= (p.Leu54=) c.-30+1681C= (n.-30+1681C=) n.350+1681C= | |
19 | g.41352883C>G | CA507690191 | TGFB1,TMEM91 | c.162G>C (p.Leu54=) c.-30+1681C>G (n.-30+1681C>G) n.350+1681C>G | gnomAD v4 |
19 | g.41352883C>T | CA507690192 | TGFB1,TMEM91 | c.162G>A (p.Leu54=) c.-30+1681C>T (n.-30+1681C>T) n.350+1681C>T | dbSNP gnomAD v4 |
19 | g.41352884A>C | CA406005886 | TGFB1,TMEM91 | c.161T>G (p.Leu54Arg) c.-30+1682A>C (n.-30+1682A>C) n.350+1682A>C | |
19 | g.41352884A>G | CA406005888 | TGFB1,TMEM91 | c.161T>C (p.Leu54Pro) c.-30+1682A>G (n.-30+1682A>G) n.350+1682A>G | gnomAD v4 |
19 | g.41352884A>T | CA406005891 | TGFB1,TMEM91 | c.161T>A (p.Leu54Gln) c.-30+1682A>T (n.-30+1682A>T) n.350+1682A>T | |
19 | g.41352885G>A | CA507690193 | TGFB1,TMEM91 | c.160C>T (p.Leu54=) c.-30+1683G>A (n.-30+1683G>A) n.350+1683G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.41352885G>C | CA406005895 | TGFB1,TMEM91 | c.160C>G (p.Leu54Val) c.-30+1683G>C (n.-30+1683G>C) n.350+1683G>C | |
19 | g.41352885G= | CA2336426148 | TGFB1,TMEM91 | c.160C= (p.Leu54=) c.-30+1683G= (n.-30+1683G=) n.350+1683G= | |
19 | g.41352885G>T | CA406005898 | TGFB1,TMEM91 | c.160C>A (p.Leu54Met) c.-30+1683G>T (n.-30+1683G>T) n.350+1683G>T | gnomAD v4 |
19 | g.41352886G>A | CA9460167 | TGFB1,TMEM91 | c.159C>T (p.Ile53=) c.-30+1684G>A (n.-30+1684G>A) n.350+1684G>A | ClinVar dbSNP ExAC gnomAD v4 |
19 | g.41352886G>C | CA406005900 | TGFB1,TMEM91 | c.159C>G (p.Ile53Met) c.-30+1684G>C (n.-30+1684G>C) n.350+1684G>C | |
19 | g.41352886G= | CA2336426149 | TGFB1,TMEM91 | c.159C= (p.Ile53=) c.-30+1684G= (n.-30+1684G=) n.350+1684G= | |
19 | g.41352886G>T | CA507690194 | TGFB1,TMEM91 | c.159C>A (p.Ile53=) c.-30+1684G>T (n.-30+1684G>T) n.350+1684G>T | gnomAD v4 |
19 | g.41352887A= | CA2336426150 | TGFB1,TMEM91 | c.158T= (p.Ile53=) c.-30+1685A= (n.-30+1685A=) n.350+1685A= | |
19 | g.41352887A>C | CA406005901 | TGFB1,TMEM91 | c.158T>G (p.Ile53Ser) c.-30+1685A>C (n.-30+1685A>C) n.350+1685A>C | gnomAD v4 |
19 | g.41352887A>G | CA9460168 | TGFB1,TMEM91 | c.158T>C (p.Ile53Thr) c.-30+1685A>G (n.-30+1685A>G) n.350+1685A>G | ClinVar dbSNP ExAC gnomAD v2 |
19 | g.41352887A>T | CA406005904 | TGFB1,TMEM91 | c.158T>A (p.Ile53Asn) c.-30+1685A>T (n.-30+1685A>T) n.350+1685A>T | |
19 | g.41352888T>A | CA406005908 | TGFB1,TMEM91 | c.157A>T (p.Ile53Phe) c.-30+1686T>A (n.-30+1686T>A) n.350+1686T>A | |
19 | g.41352888T>C | CA406005910 | TGFB1,TMEM91 | c.157A>G (p.Ile53Val) c.-30+1686T>C (n.-30+1686T>C) n.350+1686T>C | |
19 | g.41352888T>G | CA406005911 | TGFB1,TMEM91 | c.157A>C (p.Ile53Leu) c.-30+1686T>G (n.-30+1686T>G) n.350+1686T>G | |
19 | g.41352889C>A | CA406005913 | TGFB1,TMEM91 | c.156G>T (p.Gln52His) c.-30+1687C>A (n.-30+1687C>A) n.350+1687C>A | gnomAD v4 |
19 | g.41352889C>G | CA406005912 | TGFB1,TMEM91 | c.156G>C (p.Gln52His) c.-30+1687C>G (n.-30+1687C>G) n.350+1687C>G | |
19 | g.41352889C>T | CA507690195 | TGFB1,TMEM91 | c.156G>A (p.Gln52=) c.-30+1687C>T (n.-30+1687C>T) n.350+1687C>T | |
19 | g.41352890T>A | CA406005914 | TGFB1,TMEM91 | c.155A>T (p.Gln52Leu) c.-30+1688T>A (n.-30+1688T>A) n.350+1688T>A | |
19 | g.41352890T>C | CA406005921 | TGFB1,TMEM91 | c.155A>G (p.Gln52Arg) c.-30+1688T>C (n.-30+1688T>C) n.350+1688T>C | gnomAD v4 |
19 | g.41352890T>G | CA406005918 | TGFB1,TMEM91 | c.155A>C (p.Gln52Pro) c.-30+1688T>G (n.-30+1688T>G) n.350+1688T>G | |
19 | g.41352891G>A | CA406005923 | TGFB1,TMEM91 | c.154C>T (p.Gln52Ter) c.-30+1689G>A (n.-30+1689G>A) n.350+1689G>A | dbSNP gnomAD v2 |
19 | g.41352891G>C | CA406005926 | TGFB1,TMEM91 | c.154C>G (p.Gln52Glu) c.-30+1689G>C (n.-30+1689G>C) n.350+1689G>C | |
19 | g.41352891G= | CA2336426151 | TGFB1,TMEM91 | c.154C= (p.Gln52=) c.-30+1689G= (n.-30+1689G=) n.350+1689G= |