Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.18400790G>A | CA370636624 | NAT2 | c.787G>A (p.Val263Ile) c.397G>A (p.Val133Ile) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400790G>C | CA370636625 | NAT2 | c.787G>C (p.Val263Leu) c.397G>C (p.Val133Leu) | |
8 | g.18400790G= | CA1768219155 | NAT2 | c.787G= (p.Val263=) c.397G= (p.Val133=) | |
8 | g.18400790G>T | CA370636626 | NAT2 | c.787G>T (p.Val263Phe) c.397G>T (p.Val133Phe) | gnomAD v4 |
8 | g.18400791T>A | CA370636627 | NAT2 | c.788T>A (p.Val263Asp) c.398T>A (p.Val133Asp) | |
8 | g.18400791T>C | CA173519945 | NAT2 | c.788T>C (p.Val263Ala) c.398T>C (p.Val133Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400791T>G | CA370636628 | NAT2 | c.788T>G (p.Val263Gly) c.398T>G (p.Val133Gly) | gnomAD v4 |
8 | g.18400791T= | CA1768219156 | NAT2 | c.788T= (p.Val263=) c.398T= (p.Val133=) | |
8 | g.18400792T>A | CA459699776 | NAT2 | c.789T>A (p.Val263=) c.399T>A (p.Val133=) | |
8 | g.18400792T>C | CA459699778 | NAT2 | c.789T>C (p.Val263=) c.399T>C (p.Val133=) | |
8 | g.18400792T>G | CA459699780 | NAT2 | c.789T>G (p.Val263=) c.399T>G (p.Val133=) | |
8 | g.18400793G>A | CA173519946 | NAT2 | c.790G>A (p.Glu264Lys) c.400G>A (p.Glu134Lys) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
8 | g.18400793G>C | CA370636629 | NAT2 | c.790G>C (p.Glu264Gln) c.400G>C (p.Glu134Gln) | |
8 | g.18400793G= | CA1768219157 | NAT2 | c.790G= (p.Glu264=) c.400G= (p.Glu134=) | |
8 | g.18400793G>T | CA370636630 | NAT2 | c.790G>T (p.Glu264Ter) c.400G>T (p.Glu134Ter) | |
8 | g.18400797_18400799del | CA2686326443 | NAT2 | c.794_796del (p.Glu265del) c.404_406del (p.Glu135del) | gnomAD v4 |
8 | g.18400794A>C | CA370636631 | NAT2 | c.791A>C (p.Glu264Ala) c.401A>C (p.Glu134Ala) | |
8 | g.18400794A>G | CA370636632 | NAT2 | c.791A>G (p.Glu264Gly) c.401A>G (p.Glu134Gly) | |
8 | g.18400794A>T | CA370636633 | NAT2 | c.791A>T (p.Glu264Val) c.401A>T (p.Glu134Val) | |
8 | g.18400795del | CA2686326444 | NAT2 | c.792del (p.Glu265LysfsTer3) c.402del (p.Glu135LysfsTer3) | gnomAD v4 |
8 | g.18400795A>C | CA370636634 | NAT2 | c.792A>C (p.Glu264Asp) c.402A>C (p.Glu134Asp) | |
8 | g.18400795A>G | CA459699794 | NAT2 | c.792A>G (p.Glu264=) c.402A>G (p.Glu134=) | gnomAD v4 |
8 | g.18400795A>T | CA370636635 | NAT2 | c.792A>T (p.Glu264Asp) c.402A>T (p.Glu134Asp) | |
8 | g.18400796G>A | CA370636638 | NAT2 | c.793G>A (p.Glu265Lys) c.403G>A (p.Glu135Lys) | |
8 | g.18400796G>C | CA370636636 | NAT2 | c.793G>C (p.Glu265Gln) c.403G>C (p.Glu135Gln) | gnomAD v4 |
8 | g.18400796G>T | CA370636637 | NAT2 | c.793G>T (p.Glu265Ter) c.403G>T (p.Glu135Ter) | |
8 | g.18400797A>C | CA370636639 | NAT2 | c.794A>C (p.Glu265Ala) c.404A>C (p.Glu135Ala) | |
8 | g.18400797A>G | CA370636640 | NAT2 | c.794A>G (p.Glu265Gly) c.404A>G (p.Glu135Gly) | |
8 | g.18400797A>T | CA370636641 | NAT2 | c.794A>T (p.Glu265Val) c.404A>T (p.Glu135Val) | |
8 | g.18400798A>C | CA370636642 | NAT2 | c.795A>C (p.Glu265Asp) c.405A>C (p.Glu135Asp) | |
8 | g.18400798A>G | CA459699809 | NAT2 | c.795A>G (p.Glu265=) c.405A>G (p.Glu135=) | gnomAD v4 |
8 | g.18400798A>T | CA370636643 | NAT2 | c.795A>T (p.Glu265Asp) c.405A>T (p.Glu135Asp) | |
8 | g.18400799G>A | CA4651703 | NAT2 | c.796G>A (p.Val266Met) c.406G>A (p.Val136Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400799G>C | CA370636644 | NAT2 | c.796G>C (p.Val266Leu) c.406G>C (p.Val136Leu) | |
8 | g.18400799G= | CA1768219158 | NAT2 | c.796G= (p.Val266=) c.406G= (p.Val136=) | |
8 | g.18400799G>T | CA370636645 | NAT2 | c.796G>T (p.Val266Leu) c.406G>T (p.Val136Leu) | gnomAD v4 |
8 | g.18400800T>A | CA370636646 | NAT2 | c.797T>A (p.Val266Glu) c.407T>A (p.Val136Glu) | |
8 | g.18400800T>C | CA370636647 | NAT2 | c.797T>C (p.Val266Ala) c.407T>C (p.Val136Ala) | |
8 | g.18400800T>G | CA370636648 | NAT2 | c.797T>G (p.Val266Gly) c.407T>G (p.Val136Gly) | |
8 | g.18400801G>A | CA459699822 | NAT2 | c.798G>A (p.Val266=) c.408G>A (p.Val136=) | |
8 | g.18400801G>C | CA459699823 | NAT2 | c.798G>C (p.Val266=) c.408G>C (p.Val136=) | |
8 | g.18400801G>T | CA459699826 | NAT2 | c.798G>T (p.Val266=) c.408G>T (p.Val136=) | gnomAD v4 |
8 | g.18400802C>A | CA370636649 | NAT2 | c.799C>A (p.Leu267Met) c.409C>A (p.Leu137Met) | |
8 | g.18400802C>G | CA370636650 | NAT2 | c.799C>G (p.Leu267Val) c.409C>G (p.Leu137Val) | gnomAD v4 |
8 | g.18400802C>T | CA459699831 | NAT2 | c.799C>T (p.Leu267=) c.409C>T (p.Leu137=) | |
8 | g.18400803T>A | CA370636651 | NAT2 | c.800T>A (p.Leu267Gln) c.410T>A (p.Leu137Gln) | |
8 | g.18400803T>C | CA370636653 | NAT2 | c.800T>C (p.Leu267Pro) c.410T>C (p.Leu137Pro) | |
8 | g.18400803T>G | CA370636652 | NAT2 | c.800T>G (p.Leu267Arg) c.410T>G (p.Leu137Arg) | |
8 | g.18400804G>A | CA459699840 | NAT2 | c.801G>A (p.Leu267=) c.411G>A (p.Leu137=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400804G>C | CA459699838 | NAT2 | c.801G>C (p.Leu267=) c.411G>C (p.Leu137=) | gnomAD v4 |