| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.209625919G>A | CA273928 | LAMB3 | c.1705C>T (p.Arg569Ter) c.1513C>T (p.Arg505Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.209625919G>C | CA344589727 | LAMB3 | c.1705C>G (p.Arg569Gly) c.1513C>G (p.Arg505Gly) | gnomAD v4 |
| 1 | g.209625919G= | CA1143490062 | LAMB3 | c.1705C= (p.Arg569=) c.1513C= (p.Arg505=) | |
| 1 | g.209625919G>T | CA423142721 | LAMB3 | c.1705C>A (p.Arg569=) c.1513C>A (p.Arg505=) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.209625920C>A | CA344589730 | LAMB3 | c.1704G>T (p.Gln568His) c.1512G>T (p.Gln504His) | |
| 1 | g.209625920C>G | CA344589731 | LAMB3 | c.1704G>C (p.Gln568His) c.1512G>C (p.Gln504His) | gnomAD v4 |
| 1 | g.209625920C>T | CA423142722 | LAMB3 | c.1704G>A (p.Gln568=) c.1512G>A (p.Gln504=) | gnomAD v4 |
| 1 | g.209625921T>A | CA344589734 | LAMB3 | c.1703A>T (p.Gln568Leu) c.1511A>T (p.Gln504Leu) | |
| 1 | g.209625921T>C | CA1375488 | LAMB3 | c.1703A>G (p.Gln568Arg) c.1511A>G (p.Gln504Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.209625921T>G | CA344589736 | LAMB3 | c.1703A>C (p.Gln568Pro) c.1511A>C (p.Gln504Pro) | |
| 1 | g.209625921T= | CA1145228355 | LAMB3 | c.1703A= (p.Gln568=) c.1511A= (p.Gln504=) | |
| 1 | g.209625922G>A | CA344589738 | LAMB3 | c.1702C>T (p.Gln568Ter) c.1510C>T (p.Gln504Ter) | ClinVar dbSNP gnomAD v4 |
| 1 | g.209625922G>C | CA344589740 | LAMB3 | c.1702C>G (p.Gln568Glu) c.1510C>G (p.Gln504Glu) | |
| 1 | g.209625922G= | CA2484299277 | LAMB3 | c.1702C= (p.Gln568=) c.1510C= (p.Gln504=) | |
| 1 | g.209625922G>T | CA344589742 | LAMB3 | c.1702C>A (p.Gln568Lys) c.1510C>A (p.Gln504Lys) | dbSNP |
| 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) |