Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.5218346_5226066del | CA916083167 | ClinVar | ||
11 | g.5224303_5227790del | CA2499220996 | ClinVar | ||
11 | g.5225158_5227199delinsCTTAT | CA916083168 | ClinVar | ||
11 | g.5225255_5225875delinsCCTTTTCTGAGGGATGAATAAGGCATATGCATCAGGGGCTGTTGCCAATGTGCATTAGCTGTTTGCAGCCTCACCTTCTTTCATGGAGTTTAAGATATAGTGTATTTTCCCAAGGTTTGAACTAGCTCTTCATTTCTTTATGTTTTAAATGCACTGACCTCCCACATTCCCTTTTTAGTAAAATATTCAGAAATAATTTAAATACATCATTGCAATGAAAATAAATGTTTTTTATTAGGCAGAATCCAGATGCTCAAGGCCCTTCATAATATCCCCCAGTTTAGTAGTTGGACTTAGGGAACAAAGGAACCTTTAATAGAAATTGGACAGCAAGAAAGCGAGCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAGCTGTGGGAGGAAGATAAGAGGTATGAACATGATTAGCAAAAGGGCCTAGCTTGGACTCAGAATAATCCAGCCTTATCCCAACCATAAAATAAAAGCAGAATGGTAGCTGGATTGTAGCTGCTATTAGCAATATGAAACCTCTTACATCA | CA1949563432 | |||
11 | g.5225256_5225874delinsAAGTAG | CA658820845 | |||
11 | g.5225256_5225874delinsTCTACTT | CA923726280 | |||
11 | g.5225256_5225875delinsTCTACCT | CA915940749 | |||
11 | g.5225256_5225875delinsTCTACTT | CA915940716 | ClinVar dbSNP | ||
11 | g.5225388_5226007delinsTTCTTTATGTTTTAAATGCACTGACCTCCCACATTCCCTTTTTAGTAAAATATTCAGAAATAATTTAAATACATCATTGCAATGAAAATAAATGTTTTTTATTAGGCAGAATCCAGATGCTCAAGGCCCTTCATAATATCCCCCAGTTTAGTAGTTGGACTTAGGGAACAAAGGAACCTTTAATAGAAATTGGACAGCAAGAAAGCGAGCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAGCTGTGGGAGGAAGATAAGAGGTATGAACATGATTAGCAAAAGGGCCTAGCTTGGACTCAGAATAATCCAGCCTTATCCCAACCATAAAATAAAAGCAGAATGGTAGCTGGATTGTAGCTGCTATTAGCAATATGAAACCTCTTACATCAGTTACAATTTATATGCAGAAATATTTATATGCAGAGATATTGCTATTGCCTTAACCCAGAAATTATCACTGTTATTCTTTAGAATGGTGCAAAGAGGCATGATACATTGTATCATTATTGCCCTGAAAGAAA | CA1949563581 | |||
11 | g.5225389_5226007del | CA916083169 | ClinVar dbSNP | ||
11 | g.5225465_5225726delinsTGCAATGAAAATAAATGTTTTTTATTAGGCAGAATCCAGATGCTCAAGGCCCTTCATAATATCCCCCAGTTTAGTAGTTGGACTTAGGGAACAAAGGAACCTTTAATAGAAATTGGACAGCAAGAAAGCGAGCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAG | CA1949563653 | HBB | c.316_*133delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAGCTCGCTTTCTTGCTGTCCAATTTCTATTAAAGGTTCCTTTGTTCCCTAAGTCCAACTACTAAACTGGGGGATATTATGAAGGGCCTTGAGCATCTGGATTCTGCCTAATAAAAAACATTTATTTTCATTGCA (n.[c.316_*133delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAGCTCGCTTTCTTGCTGTCCAATTTCTATTAAAGGTTCCTTTGTTCCCTAAGTCCAACTACTAAACTGGGGGATATTATGAAGGGCCTTGAGCATCTGGATTCTGCCTAATAAAAAACATTTATTTTCATTGCA;Leu106=]) | |
11 | g.5225465_5225875delinsTGCAATGAAAATAAATGTTTTTTATTAGGCAGAATCCAGATGCTCAAGGCCCTTCATAATATCCCCCAGTTTAGTAGTTGGACTTAGGGAACAAAGGAACCTTTAATAGAAATTGGACAGCAAGAAAGCGAGCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAGCTGTGGGAGGAAGATAAGAGGTATGAACATGATTAGCAAAAGGGCCTAGCTTGGACTCAGAATAATCCAGCCTTATCCCAACCATAAAATAAAAGCAGAATGGTAGCTGGATTGTAGCTGCTATTAGCAATATGAAACCTCTTACATCA | CA1949563650 | HBB | c.316-149_*133delinsTGATGTAAGAGGTTTCATATTGCTAATAGCAGCTACAATCCAGCTACCATTCTGCTTTTATTTTATGGTTGGGATAAGGCTGGATTATTCTGAGTCCAAGCTAGGCCCTTTTGCTAATCATGTTCATACCTCTTATCTTCCTCCCACAGCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAGCTCGCTTTCTTGCTGTCCAATTTCTATTAAAGGTTCCTTTGTTCCCTAAGTCCAACTACTAAACTGGGGGATATTATGAAGGGCCTTGAGCATCTGGATTCTGCCTAATAAAAAACATTTATTTTCATTGCA | |
11 | g.5225466_5225726del | CA916083170 | HBB | c.316_*132del (n.[c.316_*132del;Leu106=]) | ClinVar dbSNP |
11 | g.5225467_5225876del | CA915947982 | HBB | c.316-149_*132del | ClinVar dbSNP |
11 | g.5225597_5225726delinsCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAG | CA1949564026 | HBB | c.316_*1delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAG (n.[c.316_*1delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAG;Leu106=]) c.*132_*261delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAG (n.*132_*261delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAG) | |
11 | g.5225598_5225726del | CA1139661787 | HBB | c.316_444del (p.Leu106_Ter148del) c.*132_*260del (n.*132_*260del) | ClinVar dbSNP |
11 | g.5225623_5225629delinsTTAGCCA | CA1949564337 | HBB | c.413_419delinsTGGCTAA (p.Val138=) c.*229_*235delinsTGGCTAA (n.*229_*235delinsTGGCTAA) | |
11 | g.5225624_5225629del | CA217112329 | HBB | c.413_418del (p.Val138_Asn140delinsAsp) c.*229_*234del (n.*229_*234del) | dbSNP |
11 | g.5225629_5225632del | CA2695213000 | HBB | c.411_414del (p.Val138LeufsTer20) c.*227_*230del (n.*227_*230del) | |
11 | g.5225628_5225638delinsCACACCAGCCA | CA1949564377 | HBB | c.404_414delinsTGGCTGGTGTG (p.Val135=) c.*220_*230delinsTGGCTGGTGTG (n.*220_*230delinsTGGCTGGTGTG) | |
11 | g.5225629A>C | CA379273662 | HBB | c.413T>G (p.Val138Gly) c.*229T>G (n.*229T>G) | |
11 | g.5225629A>G | CA379273663 | HBB | c.413T>C (p.Val138Ala) c.*229T>C (n.*229T>C) | |
11 | g.5225629A>T | CA379273664 | HBB | c.413T>A (p.Val138Glu) c.*229T>A (n.*229T>A) | |
11 | g.5225629_5225630delinsCA | CA2695213001 | HBB | c.412_413delinsTG (p.Val138Trp) c.*228_*229delinsTG (n.*228_*229delinsTG) | |
11 | g.5225629_5225638delinsCTGC | CA217112350 | HBB | c.404_413delinsGCAG (p.Val135_Val138delinsGlyArg) c.*220_*229delinsGCAG (n.*220_*229delinsGCAG) | dbSNP |
11 | g.5225630C>A | CA379273666 | HBB | c.412G>T (p.Val138Leu) c.*228G>T (n.*228G>T) | |
11 | g.5225630C= | CA1949564386 | HBB | c.412G= (p.Val138=) c.*228G= (n.*228G=) | |
11 | g.5225630C>G | CA379273665 | HBB | c.412G>C (p.Val138Leu) c.*228G>C (n.*228G>C) | |
11 | g.5225630C>T | CA5839689 | HBB | c.412G>A (p.Val138Met) c.*228G>A (n.*228G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.5225631A= | CA1949564388 | HBB | c.411T= (p.Gly137=) c.*227T= (n.*227T=) | |
11 | g.5225631A>C | CA5839690 | HBB | c.411T>G (p.Gly137=) c.*227T>G (n.*227T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.5225631A>G | CA472638306 | HBB | c.411T>C (p.Gly137=) c.*227T>C (n.*227T>C) | |
11 | g.5225631A>T | CA472638304 | HBB | c.411T>A (p.Gly137=) c.*227T>A (n.*227T>A) | |
11 | g.5225632C>A | CA379273667 | HBB | c.410G>T (p.Gly137Val) c.*226G>T (n.*226G>T) | |
11 | g.5225632C= | CA1949564393 | HBB | c.410G= (p.Gly137=) c.*226G= (n.*226G=) | |
11 | g.5225632C>G | CA217112353 | HBB | c.410G>C (p.Gly137Ala) c.*226G>C (n.*226G>C) | dbSNP |
11 | g.5225632C>T | CA124914 | HBB | c.410G>A (p.Gly137Asp) c.*226G>A (n.*226G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.5225633C>A | CA217112360 | HBB | c.409G>T (p.Gly137Cys) c.*225G>T (n.*225G>T) | dbSNP |
11 | g.5225633C= | CA1949564404 | HBB | c.409G= (p.Gly137=) c.*225G= (n.*225G=) | |
11 | g.5225633C>G | CA125500 | HBB | c.409G>C (p.Gly137Arg) c.*225G>C (n.*225G>C) | ClinVar dbSNP |
11 | g.5225633C>T | CA217112357 | HBB | c.409G>A (p.Gly137Ser) c.*225G>A (n.*225G>A) | dbSNP |
11 | g.5225633_5225634delinsCA | CA1949564400 | HBB | c.408_409delinsTG (p.Ala136=) c.*224_*225delinsTG (n.*224_*225delinsTG) | |
11 | g.5225634del | CA677551807 | HBB | c.408del (p.Gly137ValfsTer22) c.*224del (n.*224del) | dbSNP |
11 | g.5225634A>C | CA472638313 | HBB | c.408T>G (p.Ala136=) c.*224T>G (n.*224T>G) | |
11 | g.5225634A>G | CA472638314 | HBB | c.408T>C (p.Ala136=) c.*224T>C (n.*224T>C) | ClinVar |
11 | g.5225634A>T | CA472638316 | HBB | c.408T>A (p.Ala136=) c.*224T>A (n.*224T>A) | |
11 | g.5225634_5225645delinsAGCCACCACTTT | CA1949564412 | HBB | c.397_408delinsAAAGTGGTGGCT (p.Lys133=) c.*213_*224delinsAAAGTGGTGGCT (n.*213_*224delinsAAAGTGGTGGCT) | |
11 | g.5225635G>A | CA5839691 | HBB | c.407C>T (p.Ala136Val) c.*223C>T (n.*223C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.5225635G>C | CA379273668 | HBB | c.407C>G (p.Ala136Gly) c.*223C>G (n.*223C>G) | |
11 | g.5225635G= | CA1949564419 | HBB | c.407C= (p.Ala136=) c.*223C= (n.*223C=) |