Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.125317467A>C | CA441366365 | FAT4 | c.1056A>C (p.Val352=) c.-55+1490A>C (n.-55+1490A>C) | |
4 | g.125317467A>G | CA441366367 | FAT4 | c.1056A>G (p.Val352=) c.-55+1490A>G (n.-55+1490A>G) | gnomAD v4 |
4 | g.125317467A>T | CA441366366 | FAT4 | c.1056A>T (p.Val352=) c.-55+1490A>T (n.-55+1490A>T) | |
4 | g.125317468G>A | CA358117105 | FAT4 | c.1057G>A (p.Val353Met) c.-55+1491G>A (n.-55+1491G>A) | gnomAD v4 |
4 | g.125317468G>C | CA358117106 | FAT4 | c.1057G>C (p.Val353Leu) c.-55+1491G>C (n.-55+1491G>C) | |
4 | g.125317468G>T | CA358117107 | FAT4 | c.1057G>T (p.Val353Leu) c.-55+1491G>T (n.-55+1491G>T) | |
4 | g.125317469T>A | CA358117108 | FAT4 | c.1058T>A (p.Val353Glu) c.-55+1492T>A (n.-55+1492T>A) | |
4 | g.125317469T>C | CA3071910 | FAT4 | c.1058T>C (p.Val353Ala) c.-55+1492T>C (n.-55+1492T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317469T>G | CA358117109 | FAT4 | c.1058T>G (p.Val353Gly) c.-55+1492T>G (n.-55+1492T>G) | |
4 | g.125317469T= | CA1491599918 | FAT4 | c.1058T= (p.Val353=) c.-55+1492T= (n.-55+1492T=) | |
4 | g.125317470G>A | CA441366370 | FAT4 | c.1059G>A (p.Val353=) c.-55+1493G>A (n.-55+1493G>A) | ClinVar |
4 | g.125317470G>C | CA441366372 | FAT4 | c.1059G>C (p.Val353=) c.-55+1493G>C (n.-55+1493G>C) | |
4 | g.125317470G>T | CA441366373 | FAT4 | c.1059G>T (p.Val353=) c.-55+1493G>T (n.-55+1493G>T) | |
4 | g.125317471A>C | CA358117112 | FAT4 | c.1060A>C (p.Lys354Gln) c.-55+1494A>C (n.-55+1494A>C) | |
4 | g.125317471A>G | CA358117111 | FAT4 | c.1060A>G (p.Lys354Glu) c.-55+1494A>G (n.-55+1494A>G) | |
4 | g.125317471A>T | CA358117110 | FAT4 | c.1060A>T (p.Lys354Ter) c.-55+1494A>T (n.-55+1494A>T) | |
4 | g.125317472A>C | CA358117113 | FAT4 | c.1061A>C (p.Lys354Thr) c.-55+1495A>C (n.-55+1495A>C) | |
4 | g.125317472A>G | CA358117114 | FAT4 | c.1061A>G (p.Lys354Arg) c.-55+1495A>G (n.-55+1495A>G) | gnomAD v4 |
4 | g.125317472A>T | CA358117115 | FAT4 | c.1061A>T (p.Lys354Met) c.-55+1495A>T (n.-55+1495A>T) | |
4 | g.125317473G>A | CA3071911 | FAT4 | c.1062G>A (p.Lys354=) c.-55+1496G>A (n.-55+1496G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317473G>C | CA358117116 | FAT4 | c.1062G>C (p.Lys354Asn) c.-55+1496G>C (n.-55+1496G>C) | gnomAD v4 |
4 | g.125317473G= | CA1491599926 | FAT4 | c.1062G= (p.Lys354=) c.-55+1496G= (n.-55+1496G=) | |
4 | g.125317473G>T | CA358117117 | FAT4 | c.1062G>T (p.Lys354Asn) c.-55+1496G>T (n.-55+1496G>T) | gnomAD v4 |
4 | g.125317474T>A | CA358117118 | FAT4 | c.1063T>A (p.Phe355Ile) c.-55+1497T>A (n.-55+1497T>A) | ClinVar dbSNP gnomAD v4 |
4 | g.125317474T>C | CA358117120 | FAT4 | c.1063T>C (p.Phe355Leu) c.-55+1497T>C (n.-55+1497T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317474T>G | CA358117119 | FAT4 | c.1063T>G (p.Phe355Val) c.-55+1497T>G (n.-55+1497T>G) | |
4 | g.125317474T= | CA1491599931 | FAT4 | c.1063T= (p.Phe355=) c.-55+1497T= (n.-55+1497T=) | |
4 | g.125317475T>A | CA358117121 | FAT4 | c.1064T>A (p.Phe355Tyr) c.-55+1498T>A (n.-55+1498T>A) | |
4 | g.125317475T>C | CA358117122 | FAT4 | c.1064T>C (p.Phe355Ser) c.-55+1498T>C (n.-55+1498T>C) | |
4 | g.125317475T>G | CA358117123 | FAT4 | c.1064T>G (p.Phe355Cys) c.-55+1498T>G (n.-55+1498T>G) | |
4 | g.125317476C>A | CA358117124 | FAT4 | c.1065C>A (p.Phe355Leu) c.-55+1499C>A (n.-55+1499C>A) | |
4 | g.125317476C>G | CA358117125 | FAT4 | c.1065C>G (p.Phe355Leu) c.-55+1499C>G (n.-55+1499C>G) | |
4 | g.125317476C>T | CA441366376 | FAT4 | c.1065C>T (p.Phe355=) c.-55+1499C>T (n.-55+1499C>T) | |
4 | g.125317477C>A | CA358117126 | FAT4 | c.1066C>A (p.Arg356Ser) c.-55+1500C>A (n.-55+1500C>A) | |
4 | g.125317477C= | CA1491599935 | FAT4 | c.1066C= (p.Arg356=) c.-55+1500C= (n.-55+1500C=) | |
4 | g.125317477C>G | CA358117127 | FAT4 | c.1066C>G (p.Arg356Gly) c.-55+1500C>G (n.-55+1500C>G) | gnomAD v4 |
4 | g.125317477C>T | CA104861787 | FAT4 | c.1066C>T (p.Arg356Cys) c.-55+1500C>T (n.-55+1500C>T) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317478G>A | CA358117128 | FAT4 | c.1067G>A (p.Arg356His) c.-55+1501G>A (n.-55+1501G>A) | COSMIC COSMIC |
4 | g.125317478G>C | CA358117129 | FAT4 | c.1067G>C (p.Arg356Pro) c.-55+1501G>C (n.-55+1501G>C) | |
4 | g.125317478G>T | CA358117130 | FAT4 | c.1067G>T (p.Arg356Leu) c.-55+1501G>T (n.-55+1501G>T) | |
4 | g.125317479C>A | CA441366379 | FAT4 | c.1068C>A (p.Arg356=) c.-55+1502C>A (n.-55+1502C>A) | |
4 | g.125317479C>G | CA441366380 | FAT4 | c.1068C>G (p.Arg356=) c.-55+1502C>G (n.-55+1502C>G) | |
4 | g.125317479C>T | CA441366381 | FAT4 | c.1068C>T (p.Arg356=) c.-55+1502C>T (n.-55+1502C>T) | |
4 | g.125317480T>A | CA358117131 | FAT4 | c.1069T>A (p.Tyr357Asn) c.-55+1503T>A (n.-55+1503T>A) | |
4 | g.125317480T>C | CA358117133 | FAT4 | c.1069T>C (p.Tyr357His) c.-55+1503T>C (n.-55+1503T>C) | |
4 | g.125317480T>G | CA358117132 | FAT4 | c.1069T>G (p.Tyr357Asp) c.-55+1503T>G (n.-55+1503T>G) | |
4 | g.125317481A>C | CA358117134 | FAT4 | c.1070A>C (p.Tyr357Ser) c.-55+1504A>C (n.-55+1504A>C) | |
4 | g.125317481A>G | CA358117135 | FAT4 | c.1070A>G (p.Tyr357Cys) c.-55+1504A>G (n.-55+1504A>G) | gnomAD v4 |
4 | g.125317481A>T | CA358117136 | FAT4 | c.1070A>T (p.Tyr357Phe) c.-55+1504A>T (n.-55+1504A>T) | |
4 | g.125317482C>A | CA358117137 | FAT4 | c.1071C>A (p.Tyr357Ter) c.-55+1505C>A (n.-55+1505C>A) |