Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.209625923G>A | CA1375489 | LAMB3 | c.1701C>T (p.Cys567=) c.1509C>T (p.Cys503=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209625923G>C | CA344589745 | LAMB3 | c.1701C>G (p.Cys567Trp) c.1509C>G (p.Cys503Trp) | |
1 | g.209625923G= | CA2484299278 | LAMB3 | c.1701C= (p.Cys567=) c.1509C= (p.Cys503=) | |
1 | g.209625923G>T | CA344589747 | LAMB3 | c.1701C>A (p.Cys567Ter) c.1509C>A (p.Cys503Ter) | |
1 | g.209625924C>A | CA344589753 | LAMB3 | c.1700G>T (p.Cys567Phe) c.1508G>T (p.Cys503Phe) | |
1 | g.209625924C>G | CA344589749 | LAMB3 | c.1700G>C (p.Cys567Ser) c.1508G>C (p.Cys503Ser) | |
1 | g.209625924C>T | CA344589751 | LAMB3 | c.1700G>A (p.Cys567Tyr) c.1508G>A (p.Cys503Tyr) | |
1 | g.209625925A>C | CA344589755 | LAMB3 | c.1699T>G (p.Cys567Gly) c.1507T>G (p.Cys503Gly) | |
1 | g.209625925A>G | CA344589756 | LAMB3 | c.1699T>C (p.Cys567Arg) c.1507T>C (p.Cys503Arg) | |
1 | g.209625925A>T | CA344589758 | LAMB3 | c.1699T>A (p.Cys567Ser) c.1507T>A (p.Cys503Ser) | |
1 | g.209625926C>A | CA344589760 | LAMB3 | c.1698G>T (p.Gln566His) c.1506G>T (p.Gln502His) | |
1 | g.209625926C>G | CA344589762 | LAMB3 | c.1698G>C (p.Gln566His) c.1506G>C (p.Gln502His) | |
1 | g.209625926C>T | CA423142723 | LAMB3 | c.1698G>A (p.Gln566=) c.1506G>A (p.Gln502=) | ClinVar dbSNP COSMIC |
1 | g.209625927T>A | CA344589765 | LAMB3 | c.1697A>T (p.Gln566Leu) c.1505A>T (p.Gln502Leu) | |
1 | g.209625927T>C | CA344589768 | LAMB3 | c.1697A>G (p.Gln566Arg) c.1505A>G (p.Gln502Arg) | |
1 | g.209625927T>G | CA344589766 | LAMB3 | c.1697A>C (p.Gln566Pro) c.1505A>C (p.Gln502Pro) | |
1 | g.209625928G>A | CA344589769 | LAMB3 | c.1696C>T (p.Gln566Ter) c.1504C>T (p.Gln502Ter) | |
1 | g.209625928G>C | CA1375490 | LAMB3 | c.1696C>G (p.Gln566Glu) c.1504C>G (p.Gln502Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209625928G= | CA2484299279 | LAMB3 | c.1696C= (p.Gln566=) c.1504C= (p.Gln502=) | |
1 | g.209625928G>T | CA344589770 | LAMB3 | c.1696C>A (p.Gln566Lys) c.1504C>A (p.Gln502Lys) | |
1 | g.209625929G>A | CA423142724 | LAMB3 | c.1695C>T (p.Asp565=) c.1503C>T (p.Asp501=) | gnomAD v4 |
1 | g.209625929G>C | CA344589773 | LAMB3 | c.1695C>G (p.Asp565Glu) c.1503C>G (p.Asp501Glu) | |
1 | g.209625929G>T | CA344589774 | LAMB3 | c.1695C>A (p.Asp565Glu) c.1503C>A (p.Asp501Glu) | |
1 | g.209625930T>A | CA344589777 | LAMB3 | c.1694A>T (p.Asp565Val) c.1502A>T (p.Asp501Val) | |
1 | g.209625930T>C | CA344589778 | LAMB3 | c.1694A>G (p.Asp565Gly) c.1502A>G (p.Asp501Gly) | |
1 | g.209625930T>G | CA344589780 | LAMB3 | c.1694A>C (p.Asp565Ala) c.1502A>C (p.Asp501Ala) | gnomAD v4 |
1 | g.209625931C>A | CA344589781 | LAMB3 | c.1693G>T (p.Asp565Tyr) c.1501G>T (p.Asp501Tyr) | |
1 | g.209625931C>G | CA344589782 | LAMB3 | c.1693G>C (p.Asp565His) c.1501G>C (p.Asp501His) | |
1 | g.209625931C>T | CA344589783 | LAMB3 | c.1693G>A (p.Asp565Asn) c.1501G>A (p.Asp501Asn) | COSMIC |
1 | g.209625932A>C | CA344589784 | LAMB3 | c.1692T>G (p.Cys564Trp) c.1500T>G (p.Cys500Trp) | |
1 | g.209625932A>G | CA423142725 | LAMB3 | c.1692T>C (p.Cys564=) c.1500T>C (p.Cys500=) | |
1 | g.209625932A>T | CA344589785 | LAMB3 | c.1692T>A (p.Cys564Ter) c.1500T>A (p.Cys500Ter) | |
1 | g.209625933C>A | CA344589787 | LAMB3 | c.1691G>T (p.Cys564Phe) c.1499G>T (p.Cys500Phe) | |
1 | g.209625933C= | CA2484299280 | LAMB3 | c.1691G= (p.Cys564=) c.1499G= (p.Cys500=) | |
1 | g.209625933C>G | CA344589788 | LAMB3 | c.1691G>C (p.Cys564Ser) c.1499G>C (p.Cys500Ser) | |
1 | g.209625933C>T | CA344589790 | LAMB3 | c.1691G>A (p.Cys564Tyr) c.1499G>A (p.Cys500Tyr) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209625934A>C | CA344589791 | LAMB3 | c.1690T>G (p.Cys564Gly) c.1498T>G (p.Cys500Gly) | |
1 | g.209625934A>G | CA344589793 | LAMB3 | c.1690T>C (p.Cys564Arg) c.1498T>C (p.Cys500Arg) | |
1 | g.209625934A>T | CA344589794 | LAMB3 | c.1690T>A (p.Cys564Ser) c.1498T>A (p.Cys500Ser) | |
1 | g.209625935G>A | CA423142726 | LAMB3 | c.1689C>T (p.Arg563=) c.1497C>T (p.Arg499=) | |
1 | g.209625935G>C | CA423142727 | LAMB3 | c.1689C>G (p.Arg563=) c.1497C>G (p.Arg499=) | gnomAD v4 |
1 | g.209625935G>T | CA423142728 | LAMB3 | c.1689C>A (p.Arg563=) c.1497C>A (p.Arg499=) | |
1 | g.209625936C>A | CA344589796 | LAMB3 | c.1688G>T (p.Arg563Leu) c.1496G>T (p.Arg499Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209625936C= | CA2484299281 | LAMB3 | c.1688G= (p.Arg563=) c.1496G= (p.Arg499=) | |
1 | g.209625936C>G | CA1375492 | LAMB3 | c.1688G>C (p.Arg563Pro) c.1496G>C (p.Arg499Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209625936C>T | CA1375491 | LAMB3 | c.1688G>A (p.Arg563His) c.1496G>A (p.Arg499His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209625937G>A | CA1375493 | LAMB3 | c.1687C>T (p.Arg563Cys) c.1495C>T (p.Arg499Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209625937G>C | CA344589810 | LAMB3 | c.1687C>G (p.Arg563Gly) c.1495C>G (p.Arg499Gly) | gnomAD v4 |
1 | g.209625937G= | CA2484299282 | LAMB3 | c.1687C= (p.Arg563=) c.1495C= (p.Arg499=) | |
1 | g.209625937G>T | CA344589812 | LAMB3 | c.1687C>A (p.Arg563Ser) c.1495C>A (p.Arg499Ser) |