Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.49621991G>A | CA486349814 | MGAT2 | c.723G>A (p.Val241=) | dbSNP |
14 | g.49621991G>C | CA486349815 | MGAT2 | c.723G>C (p.Val241=) | |
14 | g.49621991G= | CA2135804767 | MGAT2 | c.723G= (p.Val241=) | |
14 | g.49621991G>T | CA486349816 | MGAT2 | c.723G>T (p.Val241=) | gnomAD v4 |
14 | g.49621992T>A | CA389620137 | MGAT2 | c.724T>A (p.Trp242Arg) | |
14 | g.49621992T>C | CA389620140 | MGAT2 | c.724T>C (p.Trp242Arg) | |
14 | g.49621992T>G | CA389620144 | MGAT2 | c.724T>G (p.Trp242Gly) | dbSNP |
14 | g.49621992T= | CA2135804768 | MGAT2 | c.724T= (p.Trp242=) | |
14 | g.49621993G>A | CA389620148 | MGAT2 | c.725G>A (p.Trp242Ter) | |
14 | g.49621993G>C | CA389620149 | MGAT2 | c.725G>C (p.Trp242Ser) | |
14 | g.49621993G>T | CA389620151 | MGAT2 | c.725G>T (p.Trp242Leu) | |
14 | g.49621994G>A | CA389620156 | MGAT2 | c.726G>A (p.Trp242Ter) | |
14 | g.49621994G>C | CA389620158 | MGAT2 | c.726G>C (p.Trp242Cys) | |
14 | g.49621994G>T | CA389620153 | MGAT2 | c.726G>T (p.Trp242Cys) | |
14 | g.49621995G>A | CA389620160 | MGAT2 | c.727G>A (p.Glu243Lys) | gnomAD v4 |
14 | g.49621995G>C | CA389620159 | MGAT2 | c.727G>C (p.Glu243Gln) | gnomAD v4 |
14 | g.49621995G>T | CA389620163 | MGAT2 | c.727G>T (p.Glu243Ter) | |
14 | g.49621996A>C | CA389620165 | MGAT2 | c.728A>C (p.Glu243Ala) | |
14 | g.49621996A>G | CA389620167 | MGAT2 | c.728A>G (p.Glu243Gly) | |
14 | g.49621996A>T | CA389620168 | MGAT2 | c.728A>T (p.Glu243Val) | |
14 | g.49621997A>C | CA389620170 | MGAT2 | c.729A>C (p.Glu243Asp) | |
14 | g.49621997A>G | CA486349824 | MGAT2 | c.729A>G (p.Glu243=) | |
14 | g.49621997A>T | CA389620171 | MGAT2 | c.729A>T (p.Glu243Asp) | |
14 | g.49621998A= | CA2135804769 | MGAT2 | c.730A= (p.Arg244=) | |
14 | g.49621998A>C | CA486349826 | MGAT2 | c.730A>C (p.Arg244=) | |
14 | g.49621998A>G | CA260660768 | MGAT2 | c.730A>G (p.Arg244Gly) | dbSNP gnomAD v4 |
14 | g.49621998A>T | CA389620175 | MGAT2 | c.730A>T (p.Arg244Ter) | |
14 | g.49621999G>A | CA389620179 | MGAT2 | c.731G>A (p.Arg244Lys) | gnomAD v4 |
14 | g.49621999G>C | CA389620180 | MGAT2 | c.731G>C (p.Arg244Thr) | |
14 | g.49621999G>T | CA389620182 | MGAT2 | c.731G>T (p.Arg244Ile) | |
14 | g.49622000A>C | CA389620184 | MGAT2 | c.732A>C (p.Arg244Ser) | gnomAD v4 |
14 | g.49622000A>G | CA486349830 | MGAT2 | c.732A>G (p.Arg244=) | |
14 | g.49622000A>T | CA389620186 | MGAT2 | c.732A>T (p.Arg244Ser) | |
14 | g.49622001G>A | CA7172594 | MGAT2 | c.733G>A (p.Val245Met) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
14 | g.49622001G>C | CA221941 | MGAT2 | c.733G>C (p.Val245Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49622001G= | CA2135804770 | MGAT2 | c.733G= (p.Val245=) | |
14 | g.49622001G>T | CA389620190 | MGAT2 | c.733G>T (p.Val245Leu) | COSMIC |
14 | g.49622002T>A | CA389620194 | MGAT2 | c.734T>A (p.Val245Glu) | |
14 | g.49622002T>C | CA389620196 | MGAT2 | c.734T>C (p.Val245Ala) | |
14 | g.49622002T>G | CA389620198 | MGAT2 | c.734T>G (p.Val245Gly) | |
14 | g.49622003G>A | CA486349833 | MGAT2 | c.735G>A (p.Val245=) | dbSNP |
14 | g.49622003G>C | CA486349834 | MGAT2 | c.735G>C (p.Val245=) | |
14 | g.49622003G= | CA2135804771 | MGAT2 | c.735G= (p.Val245=) | |
14 | g.49622003G>T | CA486349835 | MGAT2 | c.735G>T (p.Val245=) | |
14 | g.49622004A>C | CA389620201 | MGAT2 | c.736A>C (p.Lys246Gln) | |
14 | g.49622004A>G | CA389620204 | MGAT2 | c.736A>G (p.Lys246Glu) | |
14 | g.49622004A>T | CA389620207 | MGAT2 | c.736A>T (p.Lys246Ter) | |
14 | g.49622007dup | CA2624726678 | MGAT2 | c.739dup (p.Ile247AsnfsTer?) | gnomAD v4 |
14 | g.49622005A>C | CA389620210 | MGAT2 | c.737A>C (p.Lys246Thr) | |
14 | g.49622005A>G | CA389620211 | MGAT2 | c.737A>G (p.Lys246Arg) |