Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.46016329C>A | CA510650719 | MMP9,SLC12A5-AS1 | c.2085C>A (p.Gly695=) n.669-1541G>T | |
20 | g.46016329C= | CA2366481088 | MMP9,SLC12A5-AS1 | c.2085C= (p.Gly695=) n.669-1541G= | |
20 | g.46016329C>G | CA9886898 | MMP9,SLC12A5-AS1 | c.2085C>G (p.Gly695=) n.669-1541G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
20 | g.46016329C>T | CA510650722 | MMP9,SLC12A5-AS1 | c.2085C>T (p.Gly695=) n.669-1541G>A | |
20 | g.46016330T>A | CA409228086 | MMP9,SLC12A5-AS1 | c.2086T>A (p.Tyr696Asn) n.669-1542A>T | |
20 | g.46016330T>C | CA409228082 | MMP9,SLC12A5-AS1 | c.2086T>C (p.Tyr696His) n.669-1542A>G | |
20 | g.46016330T>G | CA409228079 | MMP9,SLC12A5-AS1 | c.2086T>G (p.Tyr696Asp) n.669-1542A>C | gnomAD v4 |
20 | g.46016331A>C | CA409228089 | MMP9,SLC12A5-AS1 | c.2087A>C (p.Tyr696Ser) n.669-1543T>G | |
20 | g.46016331A>G | CA409228091 | MMP9,SLC12A5-AS1 | c.2087A>G (p.Tyr696Cys) n.669-1543T>C | |
20 | g.46016331A>T | CA409228098 | MMP9,SLC12A5-AS1 | c.2087A>T (p.Tyr696Phe) n.669-1543T>A | |
20 | g.46016332C>A | CA409228101 | MMP9,SLC12A5-AS1 | c.2088C>A (p.Tyr696Ter) n.669-1544G>T | |
20 | g.46016332C= | CA2366481089 | MMP9,SLC12A5-AS1 | c.2088C= (p.Tyr696=) n.669-1544G= | |
20 | g.46016332C>G | CA409228105 | MMP9,SLC12A5-AS1 | c.2088C>G (p.Tyr696Ter) n.669-1544G>C | |
20 | g.46016332C>T | CA9886899 | MMP9,SLC12A5-AS1 | c.2088C>T (p.Tyr696=) n.669-1544G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46016333G>A | CA9886900 | MMP9,SLC12A5-AS1 | c.2089G>A (p.Val697Met) n.669-1545C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
20 | g.46016333G>C | CA409228113 | MMP9,SLC12A5-AS1 | c.2089G>C (p.Val697Leu) n.669-1545C>G | |
20 | g.46016333G= | CA2366481090 | MMP9,SLC12A5-AS1 | c.2089G= (p.Val697=) n.669-1545C= | |
20 | g.46016333G>T | CA409228111 | MMP9,SLC12A5-AS1 | c.2089G>T (p.Val697Leu) n.669-1545C>A | |
20 | g.46016333_46016336del | CA2741670584 | MMP9,SLC12A5-AS1 | c.2089_2092del (p.Val697ProfsTer?) n.669-1548_669-1545del | |
20 | g.46016334T>A | CA409228117 | MMP9,SLC12A5-AS1 | c.2090T>A (p.Val697Glu) n.669-1546A>T | |
20 | g.46016334T>C | CA409228119 | MMP9,SLC12A5-AS1 | c.2090T>C (p.Val697Ala) n.669-1546A>G | |
20 | g.46016334T>G | CA409228122 | MMP9,SLC12A5-AS1 | c.2090T>G (p.Val697Gly) n.669-1546A>C | |
20 | g.46016335G>A | CA510650738 | MMP9,SLC12A5-AS1 | c.2091G>A (p.Val697=) n.669-1547C>T | |
20 | g.46016335G>C | CA510650741 | MMP9,SLC12A5-AS1 | c.2091G>C (p.Val697=) n.669-1547C>G | gnomAD v4 |
20 | g.46016335G>T | CA510650743 | MMP9,SLC12A5-AS1 | c.2091G>T (p.Val697=) n.669-1547C>A | |
20 | g.46016336A>C | CA409228127 | MMP9,SLC12A5-AS1 | c.2092A>C (p.Thr698Pro) n.669-1548T>G | |
20 | g.46016336A>G | CA409228130 | MMP9,SLC12A5-AS1 | c.2092A>G (p.Thr698Ala) n.669-1548T>C | |
20 | g.46016336A>T | CA409228131 | MMP9,SLC12A5-AS1 | c.2092A>T (p.Thr698Ser) n.669-1548T>A | |
20 | g.46016337C>A | CA409228132 | MMP9,SLC12A5-AS1 | c.2093C>A (p.Thr698Asn) n.669-1549G>T | |
20 | g.46016337C>G | CA409228133 | MMP9,SLC12A5-AS1 | c.2093C>G (p.Thr698Ser) n.669-1549G>C | |
20 | g.46016337C>T | CA409228135 | MMP9,SLC12A5-AS1 | c.2093C>T (p.Thr698Ile) n.669-1549G>A | gnomAD v4 |
20 | g.46016338C>A | CA510650748 | MMP9,SLC12A5-AS1 | c.2094C>A (p.Thr698=) n.669-1550G>T | |
20 | g.46016338C>G | CA510650749 | MMP9,SLC12A5-AS1 | c.2094C>G (p.Thr698=) n.669-1550G>C | |
20 | g.46016338C>T | CA510650750 | MMP9,SLC12A5-AS1 | c.2094C>T (p.Thr698=) n.669-1550G>A | |
20 | g.46016339T>A | CA409228139 | MMP9,SLC12A5-AS1 | c.2095T>A (p.Tyr699Asn) n.669-1551A>T | |
20 | g.46016339T>C | CA409228142 | MMP9,SLC12A5-AS1 | c.2095T>C (p.Tyr699His) n.669-1551A>G | gnomAD v4 |
20 | g.46016339T>G | CA409228145 | MMP9,SLC12A5-AS1 | c.2095T>G (p.Tyr699Asp) n.669-1551A>C | |
20 | g.46016339_46016342del | CA2741670585 | MMP9,SLC12A5-AS1 | c.2095_2098del (p.Tyr699ThrfsTer?) n.669-1554_669-1551del | |
20 | g.46016340A>C | CA409228154 | MMP9,SLC12A5-AS1 | c.2096A>C (p.Tyr699Ser) n.669-1552T>G | |
20 | g.46016340A>G | CA409228158 | MMP9,SLC12A5-AS1 | c.2096A>G (p.Tyr699Cys) n.669-1552T>C | dbSNP gnomAD v3 |
20 | g.46016340A>T | CA409228151 | MMP9,SLC12A5-AS1 | c.2096A>T (p.Tyr699Phe) n.669-1552T>A | |
20 | g.46016341T>A | CA409228161 | MMP9,SLC12A5-AS1 | c.2097T>A (p.Tyr699Ter) n.669-1553A>T | |
20 | g.46016341T>C | CA510650759 | MMP9,SLC12A5-AS1 | c.2097T>C (p.Tyr699=) n.669-1553A>G | |
20 | g.46016341T>G | CA409228164 | MMP9,SLC12A5-AS1 | c.2097T>G (p.Tyr699Ter) n.669-1553A>C | |
20 | g.46016342G>A | CA409228168 | MMP9,SLC12A5-AS1 | c.2098G>A (p.Asp700Asn) n.669-1554C>T | |
20 | g.46016342G>C | CA409228171 | MMP9,SLC12A5-AS1 | c.2098G>C (p.Asp700His) n.669-1554C>G | |
20 | g.46016342G>T | CA409228179 | MMP9,SLC12A5-AS1 | c.2098G>T (p.Asp700Tyr) n.669-1554C>A | |
20 | g.46016343A>C | CA409228182 | MMP9,SLC12A5-AS1 | c.2099A>C (p.Asp700Ala) n.669-1555T>G | |
20 | g.46016343A>G | CA409228193 | MMP9,SLC12A5-AS1 | c.2099A>G (p.Asp700Gly) n.669-1555T>C | |
20 | g.46016343A>T | CA409228198 | MMP9,SLC12A5-AS1 | c.2099A>T (p.Asp700Val) n.669-1555T>A |