Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.81725951A>C | CA367869981 | HGF | c.1107T>G (p.Asp369Glu) c.1092T>G (p.Asp364Glu) | |
7 | g.81725951A>G | CA456129013 | HGF | c.1107T>C (p.Asp369=) c.1092T>C (p.Asp364=) | |
7 | g.81725951A>T | CA367869982 | HGF | c.1107T>A (p.Asp369Glu) c.1092T>A (p.Asp364Glu) | |
7 | g.81725952T>A | CA367869985 | HGF | c.1106A>T (p.Asp369Val) c.1091A>T (p.Asp364Val) | gnomAD v4 |
7 | g.81725952T>C | CA367869984 | HGF | c.1106A>G (p.Asp369Gly) c.1091A>G (p.Asp364Gly) | |
7 | g.81725952T>G | CA367869983 | HGF | c.1106A>C (p.Asp369Ala) c.1091A>C (p.Asp364Ala) | |
7 | g.81725953C>A | CA367869986 | HGF | c.1105G>T (p.Asp369Tyr) c.1090G>T (p.Asp364Tyr) | |
7 | g.81725953C>G | CA367869987 | HGF | c.1105G>C (p.Asp369His) c.1090G>C (p.Asp364His) | |
7 | g.81725953C>T | CA367869988 | HGF | c.1105G>A (p.Asp369Asn) c.1090G>A (p.Asp364Asn) | |
7 | g.81725954_81725966del | CA2683531047 | HGF | c.1093_1105del (p.Cys365IlefsTer?) c.1078_1090del (p.Cys360IlefsTer?) | gnomAD v4 |
7 | g.81725954A>C | CA456129014 | HGF | c.1104T>G (p.Thr368=) c.1089T>G (p.Thr363=) | |
7 | g.81725954A>G | CA456129015 | HGF | c.1104T>C (p.Thr368=) c.1089T>C (p.Thr363=) | |
7 | g.81725954A>T | CA456129016 | HGF | c.1104T>A (p.Thr368=) c.1089T>A (p.Thr363=) | |
7 | g.81725955G>A | CA367869989 | HGF | c.1103C>T (p.Thr368Ile) c.1088C>T (p.Thr363Ile) | |
7 | g.81725955G>C | CA367869990 | HGF | c.1103C>G (p.Thr368Ser) c.1088C>G (p.Thr363Ser) | |
7 | g.81725955G>T | CA367869991 | HGF | c.1103C>A (p.Thr368Asn) c.1088C>A (p.Thr363Asn) | |
7 | g.81725956T>A | CA367869992 | HGF | c.1102A>T (p.Thr368Ser) c.1087A>T (p.Thr363Ser) | |
7 | g.81725956T>C | CA367869993 | HGF | c.1102A>G (p.Thr368Ala) c.1087A>G (p.Thr363Ala) | |
7 | g.81725956T>G | CA367869994 | HGF | c.1102A>C (p.Thr368Pro) c.1087A>C (p.Thr363Pro) | |
7 | g.81725957G>A | CA456129017 | HGF | c.1101C>T (p.Thr367=) c.1086C>T (p.Thr362=) | |
7 | g.81725957G>C | CA456129018 | HGF | c.1101C>G (p.Thr367=) c.1086C>G (p.Thr362=) | |
7 | g.81725957G>T | CA456129019 | HGF | c.1101C>A (p.Thr367=) c.1086C>A (p.Thr362=) | |
7 | g.81725958G>A | CA367869995 | HGF | c.1100C>T (p.Thr367Ile) c.1085C>T (p.Thr362Ile) | dbSNP |
7 | g.81725958G>C | CA367869996 | HGF | c.1100C>G (p.Thr367Ser) c.1085C>G (p.Thr362Ser) | |
7 | g.81725958G= | CA1720883758 | HGF | c.1100C= (p.Thr367=) c.1085C= (p.Thr362=) | |
7 | g.81725958G>T | CA367869997 | HGF | c.1100C>A (p.Thr367Asn) c.1085C>A (p.Thr362Asn) | |
7 | g.81725959T>A | CA367870000 | HGF | c.1099A>T (p.Thr367Ser) c.1084A>T (p.Thr362Ser) | |
7 | g.81725959T>C | CA367869998 | HGF | c.1099A>G (p.Thr367Ala) c.1084A>G (p.Thr362Ala) | |
7 | g.81725959T>G | CA367869999 | HGF | c.1099A>C (p.Thr367Pro) c.1084A>C (p.Thr362Pro) | |
7 | g.81725960A= | CA1720883759 | HGF | c.1098T= (p.Phe366=) c.1083T= (p.Phe361=) | |
7 | g.81725960A>C | CA367870001 | HGF | c.1098T>G (p.Phe366Leu) c.1083T>G (p.Phe361Leu) | |
7 | g.81725960A>G | CA4316986 | HGF | c.1098T>C (p.Phe366=) c.1083T>C (p.Phe361=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.81725960A>T | CA367870002 | HGF | c.1098T>A (p.Phe366Leu) c.1083T>A (p.Phe361Leu) | |
7 | g.81725961A>C | CA367870003 | HGF | c.1097T>G (p.Phe366Cys) c.1082T>G (p.Phe361Cys) | |
7 | g.81725961A>G | CA367870004 | HGF | c.1097T>C (p.Phe366Ser) c.1082T>C (p.Phe361Ser) | |
7 | g.81725961A>T | CA367870005 | HGF | c.1097T>A (p.Phe366Tyr) c.1082T>A (p.Phe361Tyr) | |
7 | g.81725962A>C | CA367870006 | HGF | c.1096T>G (p.Phe366Val) c.1081T>G (p.Phe361Val) | |
7 | g.81725962A>G | CA367870007 | HGF | c.1096T>C (p.Phe366Leu) c.1081T>C (p.Phe361Leu) | |
7 | g.81725962A>T | CA367870008 | HGF | c.1096T>A (p.Phe366Ile) c.1081T>A (p.Phe361Ile) | |
7 | g.81725963A>C | CA367870009 | HGF | c.1095T>G (p.Cys365Trp) c.1080T>G (p.Cys360Trp) | |
7 | g.81725963A>G | CA456129020 | HGF | c.1095T>C (p.Cys365=) c.1080T>C (p.Cys360=) | |
7 | g.81725963A>T | CA367870010 | HGF | c.1095T>A (p.Cys365Ter) c.1080T>A (p.Cys360Ter) | |
7 | g.81725964C>A | CA367870013 | HGF | c.1094G>T (p.Cys365Phe) c.1079G>T (p.Cys360Phe) | dbSNP |
7 | g.81725964C>G | CA367870012 | HGF | c.1094G>C (p.Cys365Ser) c.1079G>C (p.Cys360Ser) | |
7 | g.81725964C>T | CA367870011 | HGF | c.1094G>A (p.Cys365Tyr) c.1079G>A (p.Cys360Tyr) | |
7 | g.81725965A>C | CA367870014 | HGF | c.1093T>G (p.Cys365Gly) c.1078T>G (p.Cys360Gly) | |
7 | g.81725965A>G | CA367870015 | HGF | c.1093T>C (p.Cys365Arg) c.1078T>C (p.Cys360Arg) | |
7 | g.81725965A>T | CA367870016 | HGF | c.1093T>A (p.Cys365Ser) c.1078T>A (p.Cys360Ser) | COSMIC |
7 | g.81725966C>A | CA367870017 | HGF | c.1092G>T (p.Trp364Cys) c.1077G>T (p.Trp359Cys) | |
7 | g.81725966C>G | CA367870018 | HGF | c.1092G>C (p.Trp364Cys) c.1077G>C (p.Trp359Cys) |