Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.59153274T>A | CA380789248 | FAM111A | c.1606T>A (p.Phe536Ile) c.1486T>A (p.Phe496Ile) | |
11 | g.59153274T>C | CA380789249 | FAM111A | c.1606T>C (p.Phe536Leu) c.1486T>C (p.Phe496Leu) | |
11 | g.59153274T>G | CA380789252 | FAM111A | c.1606T>G (p.Phe536Val) c.1486T>G (p.Phe496Val) | gnomAD v4 |
11 | g.59153275T>A | CA380789270 | FAM111A | c.1607T>A (p.Phe536Tyr) c.1487T>A (p.Phe496Tyr) | |
11 | g.59153275T>C | CA380789264 | FAM111A | c.1607T>C (p.Phe536Ser) c.1487T>C (p.Phe496Ser) | |
11 | g.59153275T>G | CA380789267 | FAM111A | c.1607T>G (p.Phe536Cys) c.1487T>G (p.Phe496Cys) | |
11 | g.59153276T>A | CA380789273 | FAM111A | c.1608T>A (p.Phe536Leu) c.1488T>A (p.Phe496Leu) | ClinVar gnomAD v4 |
11 | g.59153276T>C | CA474820240 | FAM111A | c.1608T>C (p.Phe536=) c.1488T>C (p.Phe496=) | COSMIC |
11 | g.59153276T>G | CA380789277 | FAM111A | c.1608T>G (p.Phe536Leu) c.1488T>G (p.Phe496Leu) | |
11 | g.59153277T>A | CA380789280 | FAM111A | c.1609T>A (p.Phe537Ile) c.1489T>A (p.Phe497Ile) | |
11 | g.59153277T>C | CA380789283 | FAM111A | c.1609T>C (p.Phe537Leu) c.1489T>C (p.Phe497Leu) | |
11 | g.59153277T>G | CA380789285 | FAM111A | c.1609T>G (p.Phe537Val) c.1489T>G (p.Phe497Val) | |
11 | g.59153277T= | CA1976277142 | FAM111A | c.1609T= (p.Phe537=) c.1489T= (p.Phe497=) | |
11 | g.59153278T>A | CA380789292 | FAM111A | c.1610T>A (p.Phe537Tyr) c.1490T>A (p.Phe497Tyr) | |
11 | g.59153278T>C | CA380789294 | FAM111A | c.1610T>C (p.Phe537Ser) c.1490T>C (p.Phe497Ser) | |
11 | g.59153278T>G | CA380789297 | FAM111A | c.1610T>G (p.Phe537Cys) c.1490T>G (p.Phe497Cys) | |
11 | g.59153279_59153280dup | CA6016794 | FAM111A | c.1611_1612dup (p.Phe538SerfsTer?) c.1491_1492dup (p.Phe498SerfsTer?) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.59153279del | CA2613671085 | FAM111A | c.1611del (p.Phe538LeufsTer?) c.1491del (p.Phe498LeufsTer?) | gnomAD v4 |
11 | g.59153279C>A | CA380789301 | FAM111A | c.1611C>A (p.Phe537Leu) c.1491C>A (p.Phe497Leu) | |
11 | g.59153279C>G | CA380789303 | FAM111A | c.1611C>G (p.Phe537Leu) c.1491C>G (p.Phe497Leu) | |
11 | g.59153279C>T | CA474820248 | FAM111A | c.1611C>T (p.Phe537=) c.1491C>T (p.Phe497=) | |
11 | g.59153280T>A | CA380789311 | FAM111A | c.1612T>A (p.Phe538Ile) c.1492T>A (p.Phe498Ile) | |
11 | g.59153280T>C | CA380789309 | FAM111A | c.1612T>C (p.Phe538Leu) c.1492T>C (p.Phe498Leu) | gnomAD v4 |
11 | g.59153280T>G | CA380789306 | FAM111A | c.1612T>G (p.Phe538Val) c.1492T>G (p.Phe498Val) | |
11 | g.59153281T>A | CA380789314 | FAM111A | c.1613T>A (p.Phe538Tyr) c.1493T>A (p.Phe498Tyr) | |
11 | g.59153281T>C | CA380789317 | FAM111A | c.1613T>C (p.Phe538Ser) c.1493T>C (p.Phe498Ser) | |
11 | g.59153281T>G | CA380789321 | FAM111A | c.1613T>G (p.Phe538Cys) c.1493T>G (p.Phe498Cys) | |
11 | g.59153282T>A | CA380789323 | FAM111A | c.1614T>A (p.Phe538Leu) c.1494T>A (p.Phe498Leu) | |
11 | g.59153282T>C | CA474820253 | FAM111A | c.1614T>C (p.Phe538=) c.1494T>C (p.Phe498=) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.59153282T>G | CA380789326 | FAM111A | c.1614T>G (p.Phe538Leu) c.1494T>G (p.Phe498Leu) | |
11 | g.59153282T= | CA1976277147 | FAM111A | c.1614T= (p.Phe538=) c.1494T= (p.Phe498=) | |
11 | g.59153283G>A | CA380789335 | FAM111A | c.1615G>A (p.Gly539Arg) c.1495G>A (p.Gly499Arg) | |
11 | g.59153283G>C | CA380789332 | FAM111A | c.1615G>C (p.Gly539Arg) c.1495G>C (p.Gly499Arg) | |
11 | g.59153283G>T | CA380789331 | FAM111A | c.1615G>T (p.Gly539Trp) c.1495G>T (p.Gly499Trp) | |
11 | g.59153283_59153284insAGTATACATATGGACATACTCT | CA2505695159 | FAM111A | c.1615_1616insAGTATACATATGGACATACTCT (p.Gly539GlufsTer16) c.1495_1496insAGTATACATATGGACATACTCT (p.Gly499GlufsTer16) | |
11 | g.59153284G>A | CA380789339 | FAM111A | c.1616G>A (p.Gly539Glu) c.1496G>A (p.Gly499Glu) | COSMIC |
11 | g.59153284G>C | CA380789342 | FAM111A | c.1616G>C (p.Gly539Ala) c.1496G>C (p.Gly499Ala) | |
11 | g.59153284G>T | CA380789345 | FAM111A | c.1616G>T (p.Gly539Val) c.1496G>T (p.Gly499Val) | |
11 | g.59153285G>A | CA474820260 | FAM111A | c.1617G>A (p.Gly539=) c.1497G>A (p.Gly499=) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.59153285G>C | CA474820263 | FAM111A | c.1617G>C (p.Gly539=) c.1497G>C (p.Gly499=) | |
11 | g.59153285G= | CA1976277152 | FAM111A | c.1617G= (p.Gly539=) c.1497G= (p.Gly499=) | |
11 | g.59153285G>T | CA474820264 | FAM111A | c.1617G>T (p.Gly539=) c.1497G>T (p.Gly499=) | dbSNP |
11 | g.59153286G>A | CA380789349 | FAM111A | c.1618G>A (p.Ala540Thr) c.1498G>A (p.Ala500Thr) | |
11 | g.59153286G>C | CA380789352 | FAM111A | c.1618G>C (p.Ala540Pro) c.1498G>C (p.Ala500Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.59153286G= | CA1976277154 | FAM111A | c.1618G= (p.Ala540=) c.1498G= (p.Ala500=) | |
11 | g.59153286G>T | CA380789353 | FAM111A | c.1618G>T (p.Ala540Ser) c.1498G>T (p.Ala500Ser) | |
11 | g.59153287C>A | CA380789355 | FAM111A | c.1619C>A (p.Ala540Asp) c.1499C>A (p.Ala500Asp) | dbSNP gnomAD v4 |
11 | g.59153287C= | CA1976277157 | FAM111A | c.1619C= (p.Ala540=) c.1499C= (p.Ala500=) | |
11 | g.59153287C>G | CA380789360 | FAM111A | c.1619C>G (p.Ala540Gly) c.1499C>G (p.Ala500Gly) | |
11 | g.59153287C>T | CA6016796 | FAM111A | c.1619C>T (p.Ala540Val) c.1499C>T (p.Ala500Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |