Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5218346_5226066delCA916083167 ClinVar
11g.5224303_5227790delCA2499220996 ClinVar
11g.5225158_5227199delinsCTTATCA916083168 ClinVar
11g.5225255_5225875delinsCCTTTTCTGAGGGATGAATAAGGCATATGCATCAGGGGCTGTTGCCAATGTGCATTAGCTGTTTGCAGCCTCACCTTCTTTCATGGAGTTTAAGATATAGTGTATTTTCCCAAGGTTTGAACTAGCTCTTCATTTCTTTATGTTTTAAATGCACTGACCTCCCACATTCCCTTTTTAGTAAAATATTCAGAAATAATTTAAATACATCATTGCAATGAAAATAAATGTTTTTTATTAGGCAGAATCCAGATGCTCAAGGCCCTTCATAATATCCCCCAGTTTAGTAGTTGGACTTAGGGAACAAAGGAACCTTTAATAGAAATTGGACAGCAAGAAAGCGAGCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAGCTGTGGGAGGAAGATAAGAGGTATGAACATGATTAGCAAAAGGGCCTAGCTTGGACTCAGAATAATCCAGCCTTATCCCAACCATAAAATAAAAGCAGAATGGTAGCTGGATTGTAGCTGCTATTAGCAATATGAAACCTCTTACATCACA1949563432
11g.5225256_5225874delinsAAGTAGCA658820845
11g.5225256_5225874delinsTCTACTTCA923726280
11g.5225256_5225875delinsTCTACCTCA915940749
11g.5225256_5225875delinsTCTACTTCA915940716 ClinVar dbSNP
11g.5225388_5226007delinsTTCTTTATGTTTTAAATGCACTGACCTCCCACATTCCCTTTTTAGTAAAATATTCAGAAATAATTTAAATACATCATTGCAATGAAAATAAATGTTTTTTATTAGGCAGAATCCAGATGCTCAAGGCCCTTCATAATATCCCCCAGTTTAGTAGTTGGACTTAGGGAACAAAGGAACCTTTAATAGAAATTGGACAGCAAGAAAGCGAGCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAGCTGTGGGAGGAAGATAAGAGGTATGAACATGATTAGCAAAAGGGCCTAGCTTGGACTCAGAATAATCCAGCCTTATCCCAACCATAAAATAAAAGCAGAATGGTAGCTGGATTGTAGCTGCTATTAGCAATATGAAACCTCTTACATCAGTTACAATTTATATGCAGAAATATTTATATGCAGAGATATTGCTATTGCCTTAACCCAGAAATTATCACTGTTATTCTTTAGAATGGTGCAAAGAGGCATGATACATTGTATCATTATTGCCCTGAAAGAAACA1949563581
11g.5225389_5226007delCA916083169 ClinVar dbSNP
11g.5225465_5225726delinsTGCAATGAAAATAAATGTTTTTTATTAGGCAGAATCCAGATGCTCAAGGCCCTTCATAATATCCCCCAGTTTAGTAGTTGGACTTAGGGAACAAAGGAACCTTTAATAGAAATTGGACAGCAAGAAAGCGAGCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAGCA1949563653HBBc.316_*133delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAGCTCGCTTTCTTGCTGTCCAATTTCTATTAAAGGTTCCTTTGTTCCCTAAGTCCAACTACTAAACTGGGGGATATTATGAAGGGCCTTGAGCATCTGGATTCTGCCTAATAAAAAACATTTATTTTCATTGCA (n.[c.316_*133delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAGCTCGCTTTCTTGCTGTCCAATTTCTATTAAAGGTTCCTTTGTTCCCTAAGTCCAACTACTAAACTGGGGGATATTATGAAGGGCCTTGAGCATCTGGATTCTGCCTAATAAAAAACATTTATTTTCATTGCA;Leu106=])
11g.5225465_5225875delinsTGCAATGAAAATAAATGTTTTTTATTAGGCAGAATCCAGATGCTCAAGGCCCTTCATAATATCCCCCAGTTTAGTAGTTGGACTTAGGGAACAAAGGAACCTTTAATAGAAATTGGACAGCAAGAAAGCGAGCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAGCTGTGGGAGGAAGATAAGAGGTATGAACATGATTAGCAAAAGGGCCTAGCTTGGACTCAGAATAATCCAGCCTTATCCCAACCATAAAATAAAAGCAGAATGGTAGCTGGATTGTAGCTGCTATTAGCAATATGAAACCTCTTACATCACA1949563650HBBc.316-149_*133delinsTGATGTAAGAGGTTTCATATTGCTAATAGCAGCTACAATCCAGCTACCATTCTGCTTTTATTTTATGGTTGGGATAAGGCTGGATTATTCTGAGTCCAAGCTAGGCCCTTTTGCTAATCATGTTCATACCTCTTATCTTCCTCCCACAGCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAGCTCGCTTTCTTGCTGTCCAATTTCTATTAAAGGTTCCTTTGTTCCCTAAGTCCAACTACTAAACTGGGGGATATTATGAAGGGCCTTGAGCATCTGGATTCTGCCTAATAAAAAACATTTATTTTCATTGCA
11g.5225466_5225726delCA916083170HBBc.316_*132del (n.[c.316_*132del;Leu106=])
ClinVar dbSNP
11g.5225467_5225876delCA915947982HBBc.316-149_*132del
ClinVar dbSNP
11g.5225597_5225726delinsCTTAGTGATACTTGTGGGCCAGGGCATTAGCCACACCAGCCACCACTTTCTGATAGGCAGCCTGCACTGGTGGGGTGAATTCTTTGCCAAAGTGATGGGCCAGCACACAGACCAGCACGTTGCCCAGGAGCA1949564026HBBc.316_*1delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAG (n.[c.316_*1delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAG;Leu106=])
c.*132_*261delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAG (n.*132_*261delinsCTCCTGGGCAACGTGCTGGTCTGTGTGCTGGCCCATCACTTTGGCAAAGAATTCACCCCACCAGTGCAGGCTGCCTATCAGAAAGTGGTGGCTGGTGTGGCTAATGCCCTGGCCCACAAGTATCACTAAG)
11g.5225598_5225726delCA1139661787HBBc.316_444del (p.Leu106_Ter148del)
c.*132_*260del (n.*132_*260del)
ClinVar dbSNP
11g.5225645_5225662delinsTCTGATAGGCAGCCTGCACA1949564524HBBc.380_397delinsTGCAGGCTGCCTATCAGA (p.Val127=)
c.*196_*213delinsTGCAGGCTGCCTATCAGA (n.*196_*213delinsTGCAGGCTGCCTATCAGA)
11g.5225649_5225665delCA5839693HBBc.380_396del (p.Val127GlufsTer8)
c.*196_*212del (n.*196_*212del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.5225659_5225665delinsTGCACTGCA1949564691HBBc.377_383delinsCAGTGCA (p.Pro126=)
n.309_315delinsCAGTGCA
c.*193_*199delinsCAGTGCA (n.*193_*199delinsCAGTGCA)
11g.5225661_5225666delCA217112500HBBc.377_382del (p.Pro126_Val127del)
n.309_314del
c.*193_*198del (n.*193_*198del)
dbSNP
11g.5225661_5225662delinsCACA1949564719HBBc.380_381delinsTG (p.Val127=)
n.312_313delinsTG
c.*196_*197delinsTG (n.*196_*197delinsTG)
11g.5225662delCA217112521HBBc.380del (p.Val127GlyfsTer?)
n.312del
c.*196del (n.*196del)
dbSNP
11g.5225662A=CA1949564726HBBc.380T= (p.Val127=)
n.312T=
c.*196T= (n.*196T=)
11g.5225662A>CCA125340HBBc.380T>G (p.Val127Gly)
n.312T>G
c.*196T>G (n.*196T>G)
ClinVar dbSNP gnomAD v4
11g.5225662A>GCA124740HBBc.380T>C (p.Val127Ala)
n.312T>C
c.*196T>C (n.*196T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.5225662A>TCA124912HBBc.380T>A (p.Val127Glu)
n.312T>A
c.*196T>A (n.*196T>A)
ClinVar dbSNP gnomAD v4
11g.5225662_5225664delinsACTCA1949564731HBBc.378_380delinsAGT (p.Pro126=)
n.310_312delinsAGT
c.*194_*196delinsAGT (n.*194_*196delinsAGT)
11g.5225662_5225666dupCA2695213010HBBc.376_380dup (p.Ala129CysfsTer?)
n.308_312dup
c.*192_*196dup (n.*192_*196dup)
11g.5225663delCA2695213012HBBc.379del (p.Val127CysfsTer?)
n.311del
c.*195del (n.*195del)
11g.5225663C>ACA379273693HBBc.379G>T (p.Val127Leu)
n.311G>T
c.*195G>T (n.*195G>T)
11g.5225663C=CA1949564751HBBc.379G= (p.Val127=)
n.311G=
c.*195G= (n.*195G=)
11g.5225663C>GCA125507HBBc.379G>C (p.Val127Leu)
n.311G>C
c.*195G>C (n.*195G>C)
ClinVar dbSNP gnomAD v4
11g.5225663C>TCA379273694HBBc.379G>A (p.Val127Met)
n.311G>A
c.*195G>A (n.*195G>A)
11g.5225663_5225664delCA1139661788HBBc.378_379del (p.Val127AlafsTer13)
n.310_311del
c.*194_*195del (n.*194_*195del)
ClinVar dbSNP
11g.5225663_5225664delinsCTCA1949564754HBBc.378_379delinsAG (p.Pro126=)
n.310_311delinsAG
c.*194_*195delinsAG (n.*194_*195delinsAG)
11g.5225663_5225671delinsCTGGTGGGGCA1949564746HBBc.371_379delinsCCCCACCAG (p.Thr124=)
n.303_311delinsCCCCACCAG
c.*187_*195delinsCCCCACCAG (n.*187_*195delinsCCCCACCAG)
11g.5225663_5225672delinsCTGGTGGGGTCA1949564743HBBc.370_379delinsACCCCACCAG (p.Thr124=)
n.302_311delinsACCCCACCAG
c.*186_*195delinsACCCCACCAG (n.*186_*195delinsACCCCACCAG)
11g.5225664delCA217112544HBBc.378del (p.Val127CysfsTer?)
n.310del
c.*194del (n.*194del)
ClinVar dbSNP
11g.5225664T>ACA472638405HBBc.378A>T (p.Pro126=)
n.310A>T
c.*194A>T (n.*194A>T)
ClinVar dbSNP gnomAD v4
11g.5225664T>CCA472638406HBBc.378A>G (p.Pro126=)
n.310A>G
c.*194A>G (n.*194A>G)
dbSNP
11g.5225664T>GCA472638408HBBc.378A>C (p.Pro126=)
n.310A>C
c.*194A>C (n.*194A>C)
11g.5225664T=CA1949564769HBBc.378A= (p.Pro126=)
n.310A=
c.*194A= (n.*194A=)
11g.5225667_5225669dupCA217112540HBBc.376_378dup (p.Pro126_Val127insPro)
n.308_310dup
c.*192_*194dup (n.*192_*194dup)
dbSNP
11g.5225664_5225672delCA217112548HBBc.370_378del (p.Thr124_Pro126del)
n.302_310del
c.*186_*194del (n.*186_*194del)
dbSNP
11g.5225666_5225673delCA658683671HBBc.371_378del (p.Thr124SerfsTer14)
n.303_310del
c.*187_*194del (n.*187_*194del)
ClinVar dbSNP
11g.5225665G>ACA379273695HBBc.377C>T (p.Pro126Leu)
n.309C>T
c.*193C>T (n.*193C>T)
dbSNP gnomAD v2 gnomAD v4
11g.5225665G>CCA379273696HBBc.377C>G (p.Pro126Arg)
n.309C>G
c.*193C>G (n.*193C>G)
11g.5225665G=CA1949564786HBBc.377C= (p.Pro126=)
n.309C=
c.*193C= (n.*193C=)
11g.5225665G>TCA379273697HBBc.377C>A (p.Pro126Gln)
n.309C>A
c.*193C>A (n.*193C>A)
11g.5225666G>ACA379273698HBBc.376C>T (p.Pro126Ser)
n.308C>T
c.*192C>T (n.*192C>T)

Number of alleles fetched