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.5225693_5225704dupCA217112723HBBc.338_349dup (p.Ala116_His117insArgValLeuAla)
n.270_281dup
c.*154_*165dup (n.*154_*165dup)
dbSNP
11g.5225703_5225714delCA2695213021HBBc.335_346del (p.Val112_Leu115del)
n.267_278del
c.*151_*162del (n.*151_*162del)
11g.5225700_5225706dupCA217112734HBBc.339_345dup (p.Ala116CysfsTer27)
n.271_277dup
c.*155_*161dup (n.*155_*161dup)
ClinVar dbSNP
11g.5225704C>ACA125505HBBc.338G>T (p.Cys113Phe)
n.270G>T
c.*154G>T (n.*154G>T)
ClinVar dbSNP gnomAD v4
11g.5225704C=CA1949565118HBBc.338G= (p.Cys113=)
n.270G=
c.*154G= (n.*154G=)
11g.5225704C>GCA379273733HBBc.338G>C (p.Cys113Ser)
n.270G>C
c.*154G>C (n.*154G>C)
11g.5225704C>TCA125364HBBc.338G>A (p.Cys113Tyr)
n.270G>A
c.*154G>A (n.*154G>A)
ClinVar dbSNP
11g.5225704_5225716delinsCAGACCAGCACGTCA1949565114HBBc.326_338delinsACGTGCTGGTCTG (p.Asn109=)
n.258_270delinsACGTGCTGGTCTG
c.*142_*154delinsACGTGCTGGTCTG (n.*142_*154delinsACGTGCTGGTCTG)
11g.5225706_5225810delCA2695213023HBBc.316-82_338del
n.248-82_270del
c.*132-82_*154del
11g.5225705A=CA1949565122HBBc.337T= (p.Cys113=)
n.269T=
c.*153T= (n.*153T=)
11g.5225705A>CCA379273734HBBc.337T>G (p.Cys113Gly)
n.269T>G
c.*153T>G (n.*153T>G)
dbSNP
11g.5225705A>GCA124924HBBc.337T>C (p.Cys113Arg)
n.269T>C
c.*153T>C (n.*153T>C)
ClinVar dbSNP
11g.5225705A>TCA379273735HBBc.337T>A (p.Cys113Ser)
n.269T>A
c.*153T>A (n.*153T>A)
11g.5225705_5225716delCA217112758HBBc.326_337del (p.Asn109_Cys113delinsSer)
n.258_269del
c.*142_*153del (n.*142_*153del)
dbSNP
11g.5225706G>ACA472638692HBBc.336C>T (p.Val112=)
n.268C>T
c.*152C>T (n.*152C>T)
ClinVar dbSNP
11g.5225706G>CCA472638694HBBc.336C>G (p.Val112=)
n.268C>G
c.*152C>G (n.*152C>G)
11g.5225706G=CA1949565160HBBc.336C= (p.Val112=)
n.268C=
c.*152C= (n.*152C=)
11g.5225706G>TCA472638696HBBc.336C>A (p.Val112=)
n.268C>A
c.*152C>A (n.*152C>A)
11g.5225707A=CA1949565164HBBc.335T= (p.Val112=)
n.267T=
c.*151T= (n.*151T=)
11g.5225707A>CCA379273736HBBc.335T>G (p.Val112Gly)
n.267T>G
c.*151T>G (n.*151T>G)
11g.5225707A>GCA125176HBBc.335T>C (p.Val112Ala)
n.267T>C
c.*151T>C (n.*151T>C)
ClinVar dbSNP gnomAD v4
11g.5225707A>TCA379273737HBBc.335T>A (p.Val112Asp)
n.267T>A
c.*151T>A (n.*151T>A)
11g.5225707_5225719delinsACCAGCACGTTGCCA1949565167HBBc.323_335delinsGCAACGTGCTGGT (p.Gly108=)
n.255_267delinsGCAACGTGCTGGT
c.*139_*151delinsGCAACGTGCTGGT (n.*139_*151delinsGCAACGTGCTGGT)
11g.5225708C>ACA125098HBBc.334G>T (p.Val112Phe)
n.266G>T
c.*150G>T (n.*150G>T)
ClinVar dbSNP
11g.5225708C=CA1949565171HBBc.334G= (p.Val112=)
n.266G=
c.*150G= (n.*150G=)
11g.5225708C>GCA037014HBBc.334G>C (p.Val112Leu)
n.266G>C
c.*150G>C (n.*150G>C)
ClinVar dbSNP
11g.5225708C>TCA379273738HBBc.334G>A (p.Val112Ile)
n.266G>A
c.*150G>A (n.*150G>A)
gnomAD v4
11g.5225709delCA2695213024HBBc.334del (p.Val112SerfsTer?)
n.266del
c.*150del (n.*150del)
11g.5225712_5225723delCA217112772HBBc.323_334del (p.Gly108_Leu111del)
n.255_266del
c.*139_*150del (n.*139_*150del)
dbSNP
11g.5225709C>ACA472638702HBBc.333G>T (p.Leu111=)
n.265G>T
c.*149G>T (n.*149G>T)
gnomAD v4
11g.5225709C=CA1949565182HBBc.333G= (p.Leu111=)
n.265G=
c.*149G= (n.*149G=)
11g.5225709C>GCA472638704HBBc.333G>C (p.Leu111=)
n.265G>C
c.*149G>C (n.*149G>C)
11g.5225709C>TCA472638705HBBc.333G>A (p.Leu111=)
n.265G>A
c.*149G>A (n.*149G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.5225710A=CA1949565191HBBc.332T= (p.Leu111=)
n.264T=
c.*148T= (n.*148T=)

Number of alleles fetched