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.5225620del | CA217112298 | HBB | c.424del (p.Leu142TrpfsTer17) c.*240del (n.*240del) | dbSNP |
11 | g.5225620G>A | CA125422 | HBB | c.422C>T (p.Ala141Val) c.*238C>T (n.*238C>T) | ClinVar dbSNP |
11 | g.5225620G>C | CA379273652 | HBB | c.422C>G (p.Ala141Gly) c.*238C>G (n.*238C>G) | |
11 | g.5225620G= | CA1949564306 | HBB | c.422C= (p.Ala141=) c.*238C= (n.*238C=) | |
11 | g.5225620G>T | CA124904 | HBB | c.422C>A (p.Ala141Asp) c.*238C>A (n.*238C>A) | ClinVar dbSNP |
11 | g.5225620_5225621delinsAT | CA2582341861 | HBB | c.421_422delinsAT (p.Ala141Ile) c.*237_*238delinsAT (n.*237_*238delinsAT) | ClinVar |
11 | g.5225621C>A | CA379273653 | HBB | c.421G>T (p.Ala141Ser) c.*237G>T (n.*237G>T) | |
11 | g.5225621C= | CA1949564313 | HBB | c.421G= (p.Ala141=) c.*237G= (n.*237G=) | |
11 | g.5225621C>G | CA379273654 | HBB | c.421G>C (p.Ala141Pro) c.*237G>C (n.*237G>C) | |
11 | g.5225621C>T | CA125141 | HBB | c.421G>A (p.Ala141Thr) c.*237G>A (n.*237G>A) | ClinVar dbSNP |
11 | g.5225622A= | CA1949564324 | HBB | c.420T= (p.Asn140=) c.*236T= (n.*236T=) | |
11 | g.5225622A>C | CA379273655 | HBB | c.420T>G (p.Asn140Lys) c.*236T>G (n.*236T>G) | ClinVar |
11 | g.5225622A>G | CA217112321 | HBB | c.420T>C (p.Asn140=) c.*236T>C (n.*236T>C) | dbSNP gnomAD v4 |
11 | g.5225622A>T | CA124906 | HBB | c.420T>A (p.Asn140Lys) c.*236T>A (n.*236T>A) | ClinVar dbSNP |
11 | g.5225622dup | CA2695212997 | HBB | c.420dup (p.Ala141CysfsTer25) c.*236dup (n.*236dup) | |
11 | g.5225623T>A | CA379273656 | HBB | c.419A>T (p.Asn140Ile) c.*235A>T (n.*235A>T) | |
11 | g.5225623T>C | CA379273657 | HBB | c.419A>G (p.Asn140Ser) c.*235A>G (n.*235A>G) | |
11 | g.5225623T>G | CA125470 | HBB | c.419A>C (p.Asn140Thr) c.*235A>C (n.*235A>C) | ClinVar dbSNP |
11 | g.5225623T= | CA1949564338 | HBB | c.419A= (p.Asn140=) c.*235A= (n.*235A=) | |
11 | g.5225623_5225627delinsTTAGC | CA1949564335 | HBB | c.415_419delinsGCTAA (p.Ala139=) c.*231_*235delinsGCTAA (n.*231_*235delinsGCTAA) | |
11 | g.5225623_5225629delinsTTAGCCA | CA1949564337 | HBB | c.413_419delinsTGGCTAA (p.Val138=) c.*229_*235delinsTGGCTAA (n.*229_*235delinsTGGCTAA) | |
11 | g.5225624T>A | CA125426 | HBB | c.418A>T (p.Asn140Tyr) c.*234A>T (n.*234A>T) | ClinVar dbSNP |
11 | g.5225624T>C | CA124875 | HBB | c.418A>G (p.Asn140Asp) c.*234A>G (n.*234A>G) | ClinVar dbSNP |
11 | g.5225624T>G | CA379273658 | HBB | c.418A>C (p.Asn140His) c.*234A>C (n.*234A>C) | |
11 | g.5225624T= | CA1949564347 | HBB | c.418A= (p.Asn140=) c.*234A= (n.*234A=) | |
11 | g.5225624_5225627del | CA918809822 | HBB | c.415_418del (p.Ala139MetfsTer19) c.*231_*234del (n.*231_*234del) | dbSNP |
11 | g.5225624_5225627delinsA | CA2695212998 | HBB | c.415_418delinsT (p.Ala139_Asn140delinsTyr) c.*231_*234delinsT (n.*231_*234delinsT) | |
11 | g.5225624_5225627delinsGCT | CA918809824 | HBB | c.415_418delinsAGC (p.Ala139SerfsTer20) c.*231_*234delinsAGC (n.*231_*234delinsAGC) | dbSNP |
11 | g.5225624_5225627delinsTAGC | CA1949564355 | HBB | c.415_418delinsGCTA (p.Ala139=) c.*231_*234delinsGCTA (n.*231_*234delinsGCTA) | |
11 | g.5225624_5225629del | CA217112329 | HBB | c.413_418del (p.Val138_Asn140delinsAsp) c.*229_*234del (n.*229_*234del) | dbSNP |
11 | g.5225625A= | CA1949564360 | HBB | c.417T= (p.Ala139=) c.*233T= (n.*233T=) | |
11 | g.5225625A>C | CA472638286 | HBB | c.417T>G (p.Ala139=) c.*233T>G (n.*233T>G) | |
11 | g.5225625A>G | CA472638288 | HBB | c.417T>C (p.Ala139=) c.*233T>C (n.*233T>C) | dbSNP |
11 | g.5225625A>T | CA472638290 | HBB | c.417T>A (p.Ala139=) c.*233T>A (n.*233T>A) |