Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49459187C>A | CA364405088 | MMUT | c.280G>T (p.Gly94Ter) | |
6 | g.49459187C= | CA1627396721 | MMUT | c.280G= (p.Gly94=) | |
6 | g.49459187C>G | CA364405089 | MMUT | c.280G>C (p.Gly94Arg) | |
6 | g.49459187C>T | CA234291 | MMUT | c.280G>A (p.Gly94Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49459188A>C | CA450609571 | MMUT | c.279T>G (p.Arg93=) | |
6 | g.49459188A>G | CA450609575 | MMUT | c.279T>C (p.Arg93=) | |
6 | g.49459188A>T | CA450609573 | MMUT | c.279T>A (p.Arg93=) | |
6 | g.49459189C>A | CA364405090 | MMUT | c.278G>T (p.Arg93Leu) | |
6 | g.49459189C= | CA1627396731 | MMUT | c.278G= (p.Arg93=) | |
6 | g.49459189C>G | CA364405091 | MMUT | c.278G>C (p.Arg93Pro) | |
6 | g.49459189C>T | CA249728 | MMUT | c.278G>A (p.Arg93His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.49459190G>A | CA3847146 | MMUT | c.277C>T (p.Arg93Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49459190G>C | CA364405092 | MMUT | c.277C>G (p.Arg93Gly) | |
6 | g.49459190G= | CA1627396737 | MMUT | c.277C= (p.Arg93=) | |
6 | g.49459190G>T | CA364405093 | MMUT | c.277C>A (p.Arg93Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49459191T>A | CA450609577 | MMUT | c.276A>T (p.Thr92=) | |
6 | g.49459191T>C | CA450609578 | MMUT | c.276A>G (p.Thr92=) | COSMIC |
6 | g.49459191T>G | CA450609580 | MMUT | c.276A>C (p.Thr92=) | |
6 | g.49459192G>A | CA364405094 | MMUT | c.275C>T (p.Thr92Ile) | |
6 | g.49459192G>C | CA364405096 | MMUT | c.275C>G (p.Thr92Arg) | |
6 | g.49459192G>T | CA364405097 | MMUT | c.275C>A (p.Thr92Lys) | |
6 | g.49459193T>A | CA364405098 | MMUT | c.274A>T (p.Thr92Ser) | |
6 | g.49459193T>C | CA364405099 | MMUT | c.274A>G (p.Thr92Ala) | dbSNP |
6 | g.49459193T>G | CA364405101 | MMUT | c.274A>C (p.Thr92Pro) | |
6 | g.49459193T= | CA1627396743 | MMUT | c.274A= (p.Thr92=) | |
6 | g.49459194G>A | CA450609584 | MMUT | c.273C>T (p.Phe91=) | dbSNP |
6 | g.49459194G>C | CA364405107 | MMUT | c.273C>G (p.Phe91Leu) | |
6 | g.49459194G= | CA1627396747 | MMUT | c.273C= (p.Phe91=) | |
6 | g.49459194G>T | CA364405105 | MMUT | c.273C>A (p.Phe91Leu) | |
6 | g.49459195A>C | CA364405109 | MMUT | c.272T>G (p.Phe91Cys) | |
6 | g.49459195A>G | CA364405110 | MMUT | c.272T>C (p.Phe91Ser) | |
6 | g.49459195A>T | CA364405112 | MMUT | c.272T>A (p.Phe91Tyr) | |
6 | g.49459196A>C | CA364405115 | MMUT | c.271T>G (p.Phe91Val) | |
6 | g.49459196A>G | CA364405116 | MMUT | c.271T>C (p.Phe91Leu) | |
6 | g.49459196A>T | CA364405117 | MMUT | c.271T>A (p.Phe91Ile) | |
6 | g.49459197T>A | CA450609593 | MMUT | c.270A>T (p.Pro90=) | |
6 | g.49459197T>C | CA450609591 | MMUT | c.270A>G (p.Pro90=) | |
6 | g.49459197T>G | CA450609592 | MMUT | c.270A>C (p.Pro90=) | |
6 | g.49459198G>A | CA364405119 | MMUT | c.269C>T (p.Pro90Leu) | gnomAD v4 |
6 | g.49459198G>C | CA364405121 | MMUT | c.269C>G (p.Pro90Arg) | |
6 | g.49459198G= | CA1627396750 | MMUT | c.269C= (p.Pro90=) | |
6 | g.49459198G>T | CA364405122 | MMUT | c.269C>A (p.Pro90Gln) | dbSNP |
6 | g.49459199G>A | CA364405127 | MMUT | c.268C>T (p.Pro90Ser) | |
6 | g.49459199G>C | CA364405129 | MMUT | c.268C>G (p.Pro90Ala) | |
6 | g.49459199G>T | CA364405131 | MMUT | c.268C>A (p.Pro90Thr) | |
6 | g.49459199delinsTT | CA2695206698 | MMUT | c.268delinsAA (p.Pro90AsnfsTer14) | |
6 | g.49459200C>A | CA364405133 | MMUT | c.267G>T (p.Lys89Asn) | |
6 | g.49459200C= | CA1627396754 | MMUT | c.267G= (p.Lys89=) | |
6 | g.49459200C>G | CA364405132 | MMUT | c.267G>C (p.Lys89Asn) | |
6 | g.49459200C>T | CA450609595 | MMUT | c.267G>A (p.Lys89=) | ClinVar dbSNP gnomAD v4 |