Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.81725937A= | CA1720883752 | HGF | c.1121T= (p.Val374=) c.1106T= (p.Val369=) | |
7 | g.81725937A>C | CA367869950 | HGF | c.1121T>G (p.Val374Gly) c.1106T>G (p.Val369Gly) | |
7 | g.81725937A>G | CA367869952 | HGF | c.1121T>C (p.Val374Ala) c.1106T>C (p.Val369Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81725937A>T | CA367869951 | HGF | c.1121T>A (p.Val374Asp) c.1106T>A (p.Val369Asp) | |
7 | g.81725938C>A | CA367869953 | HGF | c.1120G>T (p.Val374Phe) c.1105G>T (p.Val369Phe) | |
7 | g.81725938C>G | CA367869955 | HGF | c.1120G>C (p.Val374Leu) c.1105G>C (p.Val369Leu) | |
7 | g.81725938C>T | CA367869954 | HGF | c.1120G>A (p.Val374Ile) c.1105G>A (p.Val369Ile) | |
7 | g.81725939T>A | CA456129002 | HGF | c.1119A>T (p.Arg373=) c.1104A>T (p.Arg368=) | |
7 | g.81725939T>C | CA456129003 | HGF | c.1119A>G (p.Arg373=) c.1104A>G (p.Arg368=) | |
7 | g.81725939T>G | CA456129004 | HGF | c.1119A>C (p.Arg373=) c.1104A>C (p.Arg368=) | |
7 | g.81725940C>A | CA367869956 | HGF | c.1118G>T (p.Arg373Leu) c.1103G>T (p.Arg368Leu) | |
7 | g.81725940C= | CA1720883753 | HGF | c.1118G= (p.Arg373=) c.1103G= (p.Arg368=) | |
7 | g.81725940C>G | CA367869958 | HGF | c.1118G>C (p.Arg373Pro) c.1103G>C (p.Arg368Pro) | gnomAD v4 |
7 | g.81725940C>T | CA367869957 | HGF | c.1118G>A (p.Arg373Gln) c.1103G>A (p.Arg368Gln) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
7 | g.81725941G>A | CA367869959 | HGF | c.1117C>T (p.Arg373Ter) c.1102C>T (p.Arg368Ter) | dbSNP |
7 | g.81725941G>C | CA367869960 | HGF | c.1117C>G (p.Arg373Gly) c.1102C>G (p.Arg368Gly) | dbSNP |
7 | g.81725941G= | CA1720883754 | HGF | c.1117C= (p.Arg373=) c.1102C= (p.Arg368=) | |
7 | g.81725941G>T | CA456129006 | HGF | c.1117C>A (p.Arg373=) c.1102C>A (p.Arg368=) | |
7 | g.81725942G>A | CA456129007 | HGF | c.1116C>T (p.Ile372=) c.1101C>T (p.Ile367=) | |
7 | g.81725942G>C | CA367869961 | HGF | c.1116C>G (p.Ile372Met) c.1101C>G (p.Ile367Met) | |
7 | g.81725942G>T | CA456129008 | HGF | c.1116C>A (p.Ile372=) c.1101C>A (p.Ile367=) | |
7 | g.81725943A= | CA1720883755 | HGF | c.1115T= (p.Ile372=) c.1100T= (p.Ile367=) | |
7 | g.81725943A>C | CA367869962 | HGF | c.1115T>G (p.Ile372Ser) c.1100T>G (p.Ile367Ser) | |
7 | g.81725943A>G | CA367869963 | HGF | c.1115T>C (p.Ile372Thr) c.1100T>C (p.Ile367Thr) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.81725943A>T | CA367869964 | HGF | c.1115T>A (p.Ile372Asn) c.1100T>A (p.Ile367Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81725944T>A | CA4316985 | HGF | c.1114A>T (p.Ile372Phe) c.1099A>T (p.Ile367Phe) | dbSNP ExAC gnomAD v2 COSMIC |
7 | g.81725944T>C | CA367869965 | HGF | c.1114A>G (p.Ile372Val) c.1099A>G (p.Ile367Val) | |
7 | g.81725944T>G | CA367869966 | HGF | c.1114A>C (p.Ile372Leu) c.1099A>C (p.Ile367Leu) | |
7 | g.81725944T= | CA1720883756 | HGF | c.1114A= (p.Ile372=) c.1099A= (p.Ile367=) | |
7 | g.81725945G>A | CA456129009 | HGF | c.1113C>T (p.Asn371=) c.1098C>T (p.Asn366=) | |
7 | g.81725945G>C | CA367869967 | HGF | c.1113C>G (p.Asn371Lys) c.1098C>G (p.Asn366Lys) | |
7 | g.81725945G>T | CA367869968 | HGF | c.1113C>A (p.Asn371Lys) c.1098C>A (p.Asn366Lys) | |
7 | g.81725946T>A | CA367869971 | HGF | c.1112A>T (p.Asn371Ile) c.1097A>T (p.Asn366Ile) | COSMIC |
7 | g.81725946T>C | CA367869970 | HGF | c.1112A>G (p.Asn371Ser) c.1097A>G (p.Asn366Ser) | |
7 | g.81725946T>G | CA367869969 | HGF | c.1112A>C (p.Asn371Thr) c.1097A>C (p.Asn366Thr) | |
7 | g.81725947T>A | CA367869972 | HGF | c.1111A>T (p.Asn371Tyr) c.1096A>T (p.Asn366Tyr) | |
7 | g.81725947T>C | CA367869973 | HGF | c.1111A>G (p.Asn371Asp) c.1096A>G (p.Asn366Asp) | gnomAD v4 |
7 | g.81725947T>G | CA367869974 | HGF | c.1111A>C (p.Asn371His) c.1096A>C (p.Asn366His) | |
7 | g.81725948T>A | CA456129012 | HGF | c.1110A>T (p.Pro370=) c.1095A>T (p.Pro365=) | |
7 | g.81725948T>C | CA456129010 | HGF | c.1110A>G (p.Pro370=) c.1095A>G (p.Pro365=) | gnomAD v4 |
7 | g.81725948T>G | CA456129011 | HGF | c.1110A>C (p.Pro370=) c.1095A>C (p.Pro365=) | |
7 | g.81725949G>A | CA367869975 | HGF | c.1109C>T (p.Pro370Leu) c.1094C>T (p.Pro365Leu) | dbSNP |
7 | g.81725949G>C | CA367869976 | HGF | c.1109C>G (p.Pro370Arg) c.1094C>G (p.Pro365Arg) | |
7 | g.81725949G= | CA1720883757 | HGF | c.1109C= (p.Pro370=) c.1094C= (p.Pro365=) | |
7 | g.81725949G>T | CA367869977 | HGF | c.1109C>A (p.Pro370Gln) c.1094C>A (p.Pro365Gln) | |
7 | g.81725950G>A | CA367869978 | HGF | c.1108C>T (p.Pro370Ser) c.1093C>T (p.Pro365Ser) | dbSNP gnomAD v4 |
7 | g.81725950G>C | CA367869979 | HGF | c.1108C>G (p.Pro370Ala) c.1093C>G (p.Pro365Ala) | gnomAD v4 |
7 | g.81725950G>T | CA367869980 | HGF | c.1108C>A (p.Pro370Thr) c.1093C>A (p.Pro365Thr) | |
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=) |