Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.46016279T>A | CA409227500 | MMP9,SLC12A5-AS1 | c.2035T>A (p.Tyr679Asn) n.669-1491A>T | |
20 | g.46016279T>C | CA409227502 | MMP9,SLC12A5-AS1 | c.2035T>C (p.Tyr679His) n.669-1491A>G | dbSNP gnomAD v3 gnomAD v4 COSMIC |
20 | g.46016279T>G | CA409227505 | MMP9,SLC12A5-AS1 | c.2035T>G (p.Tyr679Asp) n.669-1491A>C | |
20 | g.46016279T= | CA2366481064 | MMP9,SLC12A5-AS1 | c.2035T= (p.Tyr679=) n.669-1491A= | |
20 | g.46016280A= | CA2366481065 | MMP9,SLC12A5-AS1 | c.2036A= (p.Tyr679=) n.669-1492T= | |
20 | g.46016280A>C | CA409227508 | MMP9,SLC12A5-AS1 | c.2036A>C (p.Tyr679Ser) n.669-1492T>G | |
20 | g.46016280A>G | CA409227510 | MMP9,SLC12A5-AS1 | c.2036A>G (p.Tyr679Cys) n.669-1492T>C | dbSNP gnomAD v4 |
20 | g.46016280A>T | CA409227522 | MMP9,SLC12A5-AS1 | c.2036A>T (p.Tyr679Phe) n.669-1492T>A | |
20 | g.46016281C>A | CA409227527 | MMP9,SLC12A5-AS1 | c.2037C>A (p.Tyr679Ter) n.669-1493G>T | |
20 | g.46016281C>G | CA409227529 | MMP9,SLC12A5-AS1 | c.2037C>G (p.Tyr679Ter) n.669-1493G>C | |
20 | g.46016281C>T | CA510650587 | MMP9,SLC12A5-AS1 | c.2037C>T (p.Tyr679=) n.669-1493G>A | |
20 | g.46016282T>A | CA409227541 | MMP9,SLC12A5-AS1 | c.2038T>A (p.Trp680Arg) n.669-1494A>T | |
20 | g.46016282T>C | CA409227538 | MMP9,SLC12A5-AS1 | c.2038T>C (p.Trp680Arg) n.669-1494A>G | gnomAD v4 |
20 | g.46016282T>G | CA409227539 | MMP9,SLC12A5-AS1 | c.2038T>G (p.Trp680Gly) n.669-1494A>C | |
20 | g.46016283G>A | CA409227542 | MMP9,SLC12A5-AS1 | c.2039G>A (p.Trp680Ter) n.669-1495C>T | |
20 | g.46016283G>C | CA409227543 | MMP9,SLC12A5-AS1 | c.2039G>C (p.Trp680Ser) n.669-1495C>G | |
20 | g.46016283G>T | CA409227546 | MMP9,SLC12A5-AS1 | c.2039G>T (p.Trp680Leu) n.669-1495C>A | |
20 | g.46016284G>A | CA409227556 | MMP9,SLC12A5-AS1 | c.2040G>A (p.Trp680Ter) n.669-1496C>T | COSMIC |
20 | g.46016284G>C | CA409227559 | MMP9,SLC12A5-AS1 | c.2040G>C (p.Trp680Cys) n.669-1496C>G | |
20 | g.46016284G>T | CA409227563 | MMP9,SLC12A5-AS1 | c.2040G>T (p.Trp680Cys) n.669-1496C>A | |
20 | g.46016285C>A | CA409227574 | MMP9,SLC12A5-AS1 | c.2041C>A (p.Arg681Ser) n.669-1497G>T | gnomAD v4 |
20 | g.46016285C= | CA2366481066 | MMP9,SLC12A5-AS1 | c.2041C= (p.Arg681=) n.669-1497G= | |
20 | g.46016285C>G | CA409227576 | MMP9,SLC12A5-AS1 | c.2041C>G (p.Arg681Gly) n.669-1497G>C | dbSNP gnomAD v2 gnomAD v4 |
20 | g.46016285C>T | CA9886881 | MMP9,SLC12A5-AS1 | c.2041C>T (p.Arg681Cys) n.669-1497G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46016286G>A | CA9886882 | MMP9,SLC12A5-AS1 | c.2042G>A (p.Arg681His) n.669-1498C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
20 | g.46016286G>C | CA409227599 | MMP9,SLC12A5-AS1 | c.2042G>C (p.Arg681Pro) n.669-1498C>G | |
20 | g.46016286G= | CA2366481067 | MMP9,SLC12A5-AS1 | c.2042G= (p.Arg681=) n.669-1498C= | |
20 | g.46016286G>T | CA409227606 | MMP9,SLC12A5-AS1 | c.2042G>T (p.Arg681Leu) n.669-1498C>A | |
20 | g.46016286dup | CA2653117264 | MMP9,SLC12A5-AS1 | c.2042dup (p.Val682ArgfsTer6) n.669-1498dup | gnomAD v4 |
20 | g.46016287C>A | CA510650599 | MMP9,SLC12A5-AS1 | c.2043C>A (p.Arg681=) n.669-1499G>T | |
20 | g.46016287C= | CA2366481068 | MMP9,SLC12A5-AS1 | c.2043C= (p.Arg681=) n.669-1499G= | |
20 | g.46016287C>G | CA510650597 | MMP9,SLC12A5-AS1 | c.2043C>G (p.Arg681=) n.669-1499G>C | |
20 | g.46016287C>T | CA9886883 | MMP9,SLC12A5-AS1 | c.2043C>T (p.Arg681=) n.669-1499G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46016287_46016289delinsCGT | CA2366481069 | MMP9,SLC12A5-AS1 | c.2043_2045delinsCGT (p.Arg681=) n.669-1501_669-1499delinsACG | |
20 | g.46016288G>A | CA9886884 | MMP9,SLC12A5-AS1 | c.2044G>A (p.Val682Met) n.669-1500C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46016288G>C | CA409227614 | MMP9,SLC12A5-AS1 | c.2044G>C (p.Val682Leu) n.669-1500C>G | gnomAD v4 |
20 | g.46016288G= | CA2366481071 | MMP9,SLC12A5-AS1 | c.2044G= (p.Val682=) n.669-1500C= | |
20 | g.46016288G>T | CA9886885 | MMP9,SLC12A5-AS1 | c.2044G>T (p.Val682Leu) n.669-1500C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
20 | g.46016289_46016290del | CA2366481070 | MMP9,SLC12A5-AS1 | c.2045_2046del (p.Val682GlufsTer5) n.669-1501_669-1500del | dbSNP |
20 | g.46016289T>A | CA409227619 | MMP9,SLC12A5-AS1 | c.2045T>A (p.Val682Glu) n.669-1501A>T | |
20 | g.46016289T>C | CA409227621 | MMP9,SLC12A5-AS1 | c.2045T>C (p.Val682Ala) n.669-1501A>G | gnomAD v4 |
20 | g.46016289T>G | CA409227622 | MMP9,SLC12A5-AS1 | c.2045T>G (p.Val682Gly) n.669-1501A>C | gnomAD v4 |
20 | g.46016290G>A | CA510650604 | MMP9,SLC12A5-AS1 | c.2046G>A (p.Val682=) n.669-1502C>T | |
20 | g.46016290G>C | CA510650606 | MMP9,SLC12A5-AS1 | c.2046G>C (p.Val682=) n.669-1502C>G | |
20 | g.46016290G>T | CA510650607 | MMP9,SLC12A5-AS1 | c.2046G>T (p.Val682=) n.669-1502C>A | |
20 | g.46016291A>C | CA409227625 | MMP9,SLC12A5-AS1 | c.2047A>C (p.Ser683Arg) n.669-1503T>G | |
20 | g.46016291A>G | CA409227627 | MMP9,SLC12A5-AS1 | c.2047A>G (p.Ser683Gly) n.669-1503T>C | |
20 | g.46016291A>T | CA409227630 | MMP9,SLC12A5-AS1 | c.2047A>T (p.Ser683Cys) n.669-1503T>A | |
20 | g.46016292G>A | CA409227635 | MMP9,SLC12A5-AS1 | c.2048G>A (p.Ser683Asn) n.669-1504C>T | gnomAD v4 |
20 | g.46016292G>C | CA409227636 | MMP9,SLC12A5-AS1 | c.2048G>C (p.Ser683Thr) n.669-1504C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |