Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.113064121A>C | CA445979390 | MCC | c.1506T>G (p.Ala502=) c.2076T>G (p.Ala692=) c.1317T>G (p.Ala439=) c.1476T>G (p.Ala492=) | |
5 | g.113064121A>G | CA445979392 | MCC | c.1506T>C (p.Ala502=) c.2076T>C (p.Ala692=) c.1317T>C (p.Ala439=) c.1476T>C (p.Ala492=) | |
5 | g.113064121A>T | CA445979393 | MCC | c.1506T>A (p.Ala502=) c.2076T>A (p.Ala692=) c.1317T>A (p.Ala439=) c.1476T>A (p.Ala492=) | |
5 | g.113064122G>A | CA3370032 | MCC | c.1505C>T (p.Ala502Val) c.2075C>T (p.Ala692Val) c.1316C>T (p.Ala439Val) c.1475C>T (p.Ala492Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.113064122G>C | CA360626290 | MCC | c.1505C>G (p.Ala502Gly) c.2075C>G (p.Ala692Gly) c.1316C>G (p.Ala439Gly) c.1475C>G (p.Ala492Gly) | dbSNP |
5 | g.113064122G= | CA1573632554 | MCC | c.1505C= (p.Ala502=) c.2075C= (p.Ala692=) c.1316C= (p.Ala439=) c.1475C= (p.Ala492=) | |
5 | g.113064122G>T | CA360626291 | MCC | c.1505C>A (p.Ala502Asp) c.2075C>A (p.Ala692Asp) c.1316C>A (p.Ala439Asp) c.1475C>A (p.Ala492Asp) | |
5 | g.113064123C>A | CA360626292 | MCC | c.1504G>T (p.Ala502Ser) c.2074G>T (p.Ala692Ser) c.1315G>T (p.Ala439Ser) c.1474G>T (p.Ala492Ser) | |
5 | g.113064123C>G | CA360626293 | MCC | c.1504G>C (p.Ala502Pro) c.2074G>C (p.Ala692Pro) c.1315G>C (p.Ala439Pro) c.1474G>C (p.Ala492Pro) | |
5 | g.113064123C>T | CA360626294 | MCC | c.1504G>A (p.Ala502Thr) c.2074G>A (p.Ala692Thr) c.1315G>A (p.Ala439Thr) c.1474G>A (p.Ala492Thr) | |
5 | g.113064124T>A | CA124994762 | MCC | c.1503A>T (p.Arg501=) c.2073A>T (p.Arg691=) c.1314A>T (p.Arg438=) c.1473A>T (p.Arg491=) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.113064124T>C | CA3370033 | MCC | c.1503A>G (p.Arg501=) c.2073A>G (p.Arg691=) c.1314A>G (p.Arg438=) c.1473A>G (p.Arg491=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.113064124T>G | CA445979398 | MCC | c.1503A>C (p.Arg501=) c.2073A>C (p.Arg691=) c.1314A>C (p.Arg438=) c.1473A>C (p.Arg491=) | |
5 | g.113064124T= | CA1573632555 | MCC | c.1503A= (p.Arg501=) c.2073A= (p.Arg691=) c.1314A= (p.Arg438=) c.1473A= (p.Arg491=) | |
5 | g.113064125C>A | CA3370034 | MCC | c.1502G>T (p.Arg501Leu) c.2072G>T (p.Arg691Leu) c.1313G>T (p.Arg438Leu) c.1472G>T (p.Arg491Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.113064125C= | CA1573632556 | MCC | c.1502G= (p.Arg501=) c.2072G= (p.Arg691=) c.1313G= (p.Arg438=) c.1472G= (p.Arg491=) | |
5 | g.113064125C>G | CA360626295 | MCC | c.1502G>C (p.Arg501Pro) c.2072G>C (p.Arg691Pro) c.1313G>C (p.Arg438Pro) c.1472G>C (p.Arg491Pro) | |
5 | g.113064125C>T | CA3370035 | MCC | c.1502G>A (p.Arg501Gln) c.2072G>A (p.Arg691Gln) c.1313G>A (p.Arg438Gln) c.1472G>A (p.Arg491Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
5 | g.113064126G>A | CA3370036 | MCC | c.1501C>T (p.Arg501Ter) c.2071C>T (p.Arg691Ter) c.1312C>T (p.Arg438Ter) c.1471C>T (p.Arg491Ter) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.113064126G>C | CA360626296 | MCC | c.1501C>G (p.Arg501Gly) c.2071C>G (p.Arg691Gly) c.1312C>G (p.Arg438Gly) c.1471C>G (p.Arg491Gly) | dbSNP gnomAD v4 |
5 | g.113064126G= | CA1573632557 | MCC | c.1501C= (p.Arg501=) c.2071C= (p.Arg691=) c.1312C= (p.Arg438=) c.1471C= (p.Arg491=) | |
5 | g.113064126G>T | CA445979402 | MCC | c.1501C>A (p.Arg501=) c.2071C>A (p.Arg691=) c.1312C>A (p.Arg438=) c.1471C>A (p.Arg491=) | gnomAD v4 |
5 | g.113064127C>A | CA360626297 | MCC | c.1500G>T (p.Lys500Asn) c.2070G>T (p.Lys690Asn) c.1311G>T (p.Lys437Asn) c.1470G>T (p.Lys490Asn) | |
5 | g.113064127C= | CA1573632558 | MCC | c.1500G= (p.Lys500=) c.2070G= (p.Lys690=) c.1311G= (p.Lys437=) c.1470G= (p.Lys490=) | |
5 | g.113064127C>G | CA360626298 | MCC | c.1500G>C (p.Lys500Asn) c.2070G>C (p.Lys690Asn) c.1311G>C (p.Lys437Asn) c.1470G>C (p.Lys490Asn) | |
5 | g.113064127C>T | CA124994788 | MCC | c.1500G>A (p.Lys500=) c.2070G>A (p.Lys690=) c.1311G>A (p.Lys437=) c.1470G>A (p.Lys490=) | dbSNP |
5 | g.113064128T>A | CA3370038 | MCC | c.1499A>T (p.Lys500Met) c.2069A>T (p.Lys690Met) c.1310A>T (p.Lys437Met) c.1469A>T (p.Lys490Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.113064128T>C | CA3370037 | MCC | c.1499A>G (p.Lys500Arg) c.2069A>G (p.Lys690Arg) c.1310A>G (p.Lys437Arg) c.1469A>G (p.Lys490Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.113064128T>G | CA360626299 | MCC | c.1499A>C (p.Lys500Thr) c.2069A>C (p.Lys690Thr) c.1310A>C (p.Lys437Thr) c.1469A>C (p.Lys490Thr) | gnomAD v4 |
5 | g.113064128T= | CA1573632559 | MCC | c.1499A= (p.Lys500=) c.2069A= (p.Lys690=) c.1310A= (p.Lys437=) c.1469A= (p.Lys490=) | |
5 | g.113064129T>A | CA360626300 | MCC | c.1498A>T (p.Lys500Ter) c.2068A>T (p.Lys690Ter) c.1309A>T (p.Lys437Ter) c.1468A>T (p.Lys490Ter) | |
5 | g.113064129T>C | CA3370039 | MCC | c.1498A>G (p.Lys500Glu) c.2068A>G (p.Lys690Glu) c.1309A>G (p.Lys437Glu) c.1468A>G (p.Lys490Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.113064129T>G | CA360626301 | MCC | c.1498A>C (p.Lys500Gln) c.2068A>C (p.Lys690Gln) c.1309A>C (p.Lys437Gln) c.1468A>C (p.Lys490Gln) | |
5 | g.113064129T= | CA1573632560 | MCC | c.1498A= (p.Lys500=) c.2068A= (p.Lys690=) c.1309A= (p.Lys437=) c.1468A= (p.Lys490=) | |
5 | g.113064130G>A | CA3370040 | MCC | c.1497C>T (p.Leu499=) c.2067C>T (p.Leu689=) c.1308C>T (p.Leu436=) c.1467C>T (p.Leu489=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.113064130G>C | CA445979404 | MCC | c.1497C>G (p.Leu499=) c.2067C>G (p.Leu689=) c.1308C>G (p.Leu436=) c.1467C>G (p.Leu489=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.113064130G= | CA1573632561 | MCC | c.1497C= (p.Leu499=) c.2067C= (p.Leu689=) c.1308C= (p.Leu436=) c.1467C= (p.Leu489=) | |
5 | g.113064130G>T | CA445979405 | MCC | c.1497C>A (p.Leu499=) c.2067C>A (p.Leu689=) c.1308C>A (p.Leu436=) c.1467C>A (p.Leu489=) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.113064131A>C | CA360626302 | MCC | c.1496T>G (p.Leu499Arg) c.2066T>G (p.Leu689Arg) c.1307T>G (p.Leu436Arg) c.1466T>G (p.Leu489Arg) | |
5 | g.113064131A>G | CA360626303 | MCC | c.1496T>C (p.Leu499Pro) c.2066T>C (p.Leu689Pro) c.1307T>C (p.Leu436Pro) c.1466T>C (p.Leu489Pro) | |
5 | g.113064131A>T | CA360626304 | MCC | c.1496T>A (p.Leu499His) c.2066T>A (p.Leu689His) c.1307T>A (p.Leu436His) c.1466T>A (p.Leu489His) | |
5 | g.113064132G>A | CA124994800 | MCC | c.1495C>T (p.Leu499Phe) c.2065C>T (p.Leu689Phe) c.1306C>T (p.Leu436Phe) c.1465C>T (p.Leu489Phe) | dbSNP gnomAD v4 |
5 | g.113064132G>C | CA360626305 | MCC | c.1495C>G (p.Leu499Val) c.2065C>G (p.Leu689Val) c.1306C>G (p.Leu436Val) c.1465C>G (p.Leu489Val) | |
5 | g.113064132G= | CA1573632562 | MCC | c.1495C= (p.Leu499=) c.2065C= (p.Leu689=) c.1306C= (p.Leu436=) c.1465C= (p.Leu489=) | |
5 | g.113064132G>T | CA360626306 | MCC | c.1495C>A (p.Leu499Ile) c.2065C>A (p.Leu689Ile) c.1306C>A (p.Leu436Ile) c.1465C>A (p.Leu489Ile) | |
5 | g.113064133C>A | CA360626307 | MCC | c.1494G>T (p.Met498Ile) c.2064G>T (p.Met688Ile) c.1305G>T (p.Met435Ile) c.1464G>T (p.Met488Ile) | |
5 | g.113064133C>G | CA360626309 | MCC | c.1494G>C (p.Met498Ile) c.2064G>C (p.Met688Ile) c.1305G>C (p.Met435Ile) c.1464G>C (p.Met488Ile) | |
5 | g.113064133C>T | CA360626308 | MCC | c.1494G>A (p.Met498Ile) c.2064G>A (p.Met688Ile) c.1305G>A (p.Met435Ile) c.1464G>A (p.Met488Ile) | gnomAD v4 |
5 | g.113064134A>C | CA360626310 | MCC | c.1493T>G (p.Met498Arg) c.2063T>G (p.Met688Arg) c.1304T>G (p.Met435Arg) c.1463T>G (p.Met488Arg) | |
5 | g.113064134A>G | CA360626311 | MCC | c.1493T>C (p.Met498Thr) c.2063T>C (p.Met688Thr) c.1304T>C (p.Met435Thr) c.1463T>C (p.Met488Thr) |