Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.79599040C>A | CA396535070 | MAF | c.863G>T (p.Arg288Leu) n.2913G>T | |
16 | g.79599040C= | CA2235930976 | MAF | c.863G= (p.Arg288=) n.2913G= | |
16 | g.79599040C>G | CA122972 | MAF | c.863G>C (p.Arg288Pro) n.2913G>C | ClinVar dbSNP |
16 | g.79599040C>T | CA8184015 | MAF | c.863G>A (p.Arg288Gln) n.2913G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.79599041G>A | CA396535071 | MAF | c.862C>T (p.Arg288Trp) n.2912C>T | dbSNP gnomAD v4 |
16 | g.79599041G>C | CA396535072 | MAF | c.862C>G (p.Arg288Gly) n.2912C>G | ClinVar |
16 | g.79599041G= | CA2235930985 | MAF | c.862C= (p.Arg288=) n.2912C= | |
16 | g.79599041G>T | CA8184016 | MAF | c.862C>A (p.Arg288=) n.2912C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.79599042G>A | CA8184017 | MAF | c.861C>T (p.Ile287=) n.2911C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79599042G>C | CA8184018 | MAF | c.861C>G (p.Ile287Met) n.2911C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79599042G= | CA2235930994 | MAF | c.861C= (p.Ile287=) n.2911C= | |
16 | g.79599042G>T | CA496509092 | MAF | c.861C>A (p.Ile287=) n.2911C>A | gnomAD v4 |
16 | g.79599043A= | CA2235930997 | MAF | c.860T= (p.Ile287=) n.2910T= | |
16 | g.79599043A>C | CA8184019 | MAF | c.860T>G (p.Ile287Ser) n.2910T>G | ClinVar dbSNP ExAC gnomAD v2 |
16 | g.79599043A>G | CA396535073 | MAF | c.860T>C (p.Ile287Thr) n.2910T>C | gnomAD v4 |
16 | g.79599043A>T | CA396535074 | MAF | c.860T>A (p.Ile287Asn) n.2910T>A | |
16 | g.79599044T>A | CA396535075 | MAF | c.859A>T (p.Ile287Phe) n.2909A>T | |
16 | g.79599044T>C | CA396535076 | MAF | c.859A>G (p.Ile287Val) n.2909A>G | gnomAD v4 |
16 | g.79599044T>G | CA396535077 | MAF | c.859A>C (p.Ile287Leu) n.2909A>C | |
16 | g.79599045C>A | CA496509099 | MAF | c.858G>T (p.Val286=) n.2908G>T | |
16 | g.79599045C>G | CA496509104 | MAF | c.858G>C (p.Val286=) n.2908G>C | |
16 | g.79599045C>T | CA496509105 | MAF | c.858G>A (p.Val286=) n.2908G>A | gnomAD v4 |
16 | g.79599046A= | CA2235931000 | MAF | c.857T= (p.Val286=) n.2907T= | |
16 | g.79599046A>C | CA396535078 | MAF | c.857T>G (p.Val286Gly) n.2907T>G | dbSNP |
16 | g.79599046A>G | CA396535079 | MAF | c.857T>C (p.Val286Ala) n.2907T>C | |
16 | g.79599046A>T | CA396535080 | MAF | c.857T>A (p.Val286Glu) n.2907T>A | dbSNP |
16 | g.79599047C>A | CA396535081 | MAF | c.856G>T (p.Val286Leu) n.2906G>T | |
16 | g.79599047C>G | CA396535082 | MAF | c.856G>C (p.Val286Leu) n.2906G>C | |
16 | g.79599047C>T | CA396535083 | MAF | c.856G>A (p.Val286Met) n.2906G>A | |
16 | g.79599053_79599055del | CA2695197684 | MAF | c.854_856del (p.Glu285del) n.2904_2906del | ClinVar |
16 | g.79599048C>A | CA396535084 | MAF | c.855G>T (p.Glu285Asp) n.2905G>T | |
16 | g.79599048C>G | CA396535085 | MAF | c.855G>C (p.Glu285Asp) n.2905G>C | |
16 | g.79599048C>T | CA496509112 | MAF | c.855G>A (p.Glu285=) n.2905G>A | gnomAD v4 |
16 | g.79599049T>A | CA396535086 | MAF | c.854A>T (p.Glu285Val) n.2904A>T | |
16 | g.79599049T>C | CA396535087 | MAF | c.854A>G (p.Glu285Gly) n.2904A>G | |
16 | g.79599049T>G | CA396535088 | MAF | c.854A>C (p.Glu285Ala) n.2904A>C | |
16 | g.79599050C>A | CA396535089 | MAF | c.853G>T (p.Glu285Ter) n.2903G>T | |
16 | g.79599050C= | CA2235931003 | MAF | c.853G= (p.Glu285=) n.2903G= | |
16 | g.79599050C>G | CA396535090 | MAF | c.853G>C (p.Glu285Gln) n.2903G>C | dbSNP |
16 | g.79599050C>T | CA396535091 | MAF | c.853G>A (p.Glu285Lys) n.2903G>A | |
16 | g.79599051C>A | CA396535092 | MAF | c.852G>T (p.Glu284Asp) n.2902G>T | |
16 | g.79599051C>G | CA396535093 | MAF | c.852G>C (p.Glu284Asp) n.2902G>C | |
16 | g.79599051C>T | CA496509118 | MAF | c.852G>A (p.Glu284=) n.2902G>A | |
16 | g.79599052T>A | CA396535094 | MAF | c.851A>T (p.Glu284Val) n.2901A>T | |
16 | g.79599052T>C | CA396535095 | MAF | c.851A>G (p.Glu284Gly) n.2901A>G | dbSNP |
16 | g.79599052T>G | CA396535096 | MAF | c.851A>C (p.Glu284Ala) n.2901A>C | gnomAD v4 |
16 | g.79599052T= | CA2235931006 | MAF | c.851A= (p.Glu284=) n.2901A= | |
16 | g.79599053C>A | CA396535098 | MAF | c.850G>T (p.Glu284Ter) n.2900G>T | gnomAD v4 |
16 | g.79599053C= | CA2235931010 | MAF | c.850G= (p.Glu284=) n.2900G= | |
16 | g.79599053C>G | CA8184020 | MAF | c.850G>C (p.Glu284Gln) n.2900G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |