Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.10638161A= | CA2247331034 | MYH3 | c.3611T= (p.Leu1204=) | |
17 | g.10638161A>C | CA398151082 | MYH3 | c.3611T>G (p.Leu1204Arg) | |
17 | g.10638161A>G | CA16043037 | MYH3 | c.3611T>C (p.Leu1204Pro) | ClinVar dbSNP |
17 | g.10638161A>T | CA398151091 | MYH3 | c.3611T>A (p.Leu1204His) | |
17 | g.10638162G>A | CA287783772 | MYH3 | c.3610C>T (p.Leu1204Phe) | dbSNP gnomAD v4 |
17 | g.10638162G>C | CA398151096 | MYH3 | c.3610C>G (p.Leu1204Val) | |
17 | g.10638162G= | CA2247331037 | MYH3 | c.3610C= (p.Leu1204=) | |
17 | g.10638162G>T | CA398151099 | MYH3 | c.3610C>A (p.Leu1204Ile) | |
17 | g.10638163C>A | CA398151102 | MYH3 | c.3609G>T (p.Glu1203Asp) | |
17 | g.10638163C= | CA2247331040 | MYH3 | c.3609G= (p.Glu1203=) | |
17 | g.10638163C>G | CA287783778 | MYH3 | c.3609G>C (p.Glu1203Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.10638163C>T | CA8392464 | MYH3 | c.3609G>A (p.Glu1203=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.10638164T>A | CA398151104 | MYH3 | c.3608A>T (p.Glu1203Val) | COSMIC |
17 | g.10638164T>C | CA398151105 | MYH3 | c.3608A>G (p.Glu1203Gly) | |
17 | g.10638164T>G | CA398151106 | MYH3 | c.3608A>C (p.Glu1203Ala) | |
17 | g.10638165C>A | CA398151110 | MYH3 | c.3607G>T (p.Glu1203Ter) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.10638165C= | CA2247331043 | MYH3 | c.3607G= (p.Glu1203=) | |
17 | g.10638165C>G | CA398151112 | MYH3 | c.3607G>C (p.Glu1203Gln) | dbSNP |
17 | g.10638165C>T | CA398151108 | MYH3 | c.3607G>A (p.Glu1203Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.10638166G>A | CA8392465 | MYH3 | c.3606C>T (p.Ala1202=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.10638166G>C | CA497978533 | MYH3 | c.3606C>G (p.Ala1202=) | |
17 | g.10638166G= | CA2247331045 | MYH3 | c.3606C= (p.Ala1202=) | |
17 | g.10638166G>T | CA497978532 | MYH3 | c.3606C>A (p.Ala1202=) | gnomAD v4 |
17 | g.10638167G>A | CA398151117 | MYH3 | c.3605C>T (p.Ala1202Val) | |
17 | g.10638167G>C | CA398151121 | MYH3 | c.3605C>G (p.Ala1202Gly) | |
17 | g.10638167G>T | CA398151128 | MYH3 | c.3605C>A (p.Ala1202Asp) | |
17 | g.10638168C>A | CA398151131 | MYH3 | c.3604G>T (p.Ala1202Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.10638168C= | CA2247331047 | MYH3 | c.3604G= (p.Ala1202=) | |
17 | g.10638168C>G | CA398151132 | MYH3 | c.3604G>C (p.Ala1202Pro) | |
17 | g.10638168C>T | CA398151134 | MYH3 | c.3604G>A (p.Ala1202Thr) | |
17 | g.10638169C>A | CA497978536 | MYH3 | c.3603G>T (p.Val1201=) | dbSNP |
17 | g.10638169C= | CA2247331049 | MYH3 | c.3603G= (p.Val1201=) | |
17 | g.10638169C>G | CA497978535 | MYH3 | c.3603G>C (p.Val1201=) | |
17 | g.10638169C>T | CA497978534 | MYH3 | c.3603G>A (p.Val1201=) | |
17 | g.10638170A>C | CA398151144 | MYH3 | c.3602T>G (p.Val1201Gly) | |
17 | g.10638170A>G | CA398151139 | MYH3 | c.3602T>C (p.Val1201Ala) | |
17 | g.10638170A>T | CA398151141 | MYH3 | c.3602T>A (p.Val1201Glu) | |
17 | g.10638171C>A | CA398151147 | MYH3 | c.3601G>T (p.Val1201Leu) | |
17 | g.10638171C>G | CA398151148 | MYH3 | c.3601G>C (p.Val1201Leu) | |
17 | g.10638171C>T | CA398151149 | MYH3 | c.3601G>A (p.Val1201Met) | |
17 | g.10638172A>C | CA398151152 | MYH3 | c.3600T>G (p.Ser1200Arg) | |
17 | g.10638172A>G | CA497978702 | MYH3 | c.3600T>C (p.Ser1200=) | gnomAD v4 |
17 | g.10638172A>T | CA398151155 | MYH3 | c.3600T>A (p.Ser1200Arg) | |
17 | g.10638173C>A | CA398151156 | MYH3 | c.3599G>T (p.Ser1200Ile) | gnomAD v4 |
17 | g.10638173C>G | CA398151163 | MYH3 | c.3599G>C (p.Ser1200Thr) | |
17 | g.10638173C>T | CA398151159 | MYH3 | c.3599G>A (p.Ser1200Asn) | |
17 | g.10638174T>A | CA398151165 | MYH3 | c.3598A>T (p.Ser1200Cys) | |
17 | g.10638174T>C | CA8392466 | MYH3 | c.3598A>G (p.Ser1200Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.10638174T>G | CA398151177 | MYH3 | c.3598A>C (p.Ser1200Arg) | |
17 | g.10638174T= | CA2247331050 | MYH3 | c.3598A= (p.Ser1200=) |