Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.118436551C>ACA477086331KMT2Ac.39C>A (p.Pro13=)
c.-798-32224C>A (n.-798-32224C>A)
c.214-11074C>A (n.214-11074C>A)
 dbSNP gnomAD v4
11g.118436551C=CA2003502123KMT2Ac.39C= (p.Pro13=)
c.-798-32224C= (n.-798-32224C=)
c.214-11074C= (n.214-11074C=)
11g.118436551C>GCA477086335KMT2Ac.39C>G (p.Pro13=)
c.-798-32224C>G (n.-798-32224C>G)
c.214-11074C>G (n.214-11074C>G)
11g.118436551C>TCA477086333KMT2Ac.39C>T (p.Pro13=)
c.-798-32224C>T (n.-798-32224C>T)
c.214-11074C>T (n.214-11074C>T)
 dbSNP gnomAD v2 gnomAD v4
11g.118436552G>ACA382796833KMT2Ac.40G>A (p.Gly14Arg)
c.-798-32223G>A (n.-798-32223G>A)
c.214-11073G>A (n.214-11073G>A)
 gnomAD v4
11g.118436552G>CCA382796835KMT2Ac.40G>C (p.Gly14Arg)
c.-798-32223G>C (n.-798-32223G>C)
c.214-11073G>C (n.214-11073G>C)
11g.118436552G>TCA382796838KMT2Ac.40G>T (p.Gly14Trp)
c.-798-32223G>T (n.-798-32223G>T)
c.214-11073G>T (n.214-11073G>T)
 gnomAD v4
11g.118436554delCA2616260546KMT2Ac.42del (p.Thr15ProfsTer13)
c.-798-32221del (n.-798-32221del)
c.214-11071del (n.214-11071del)
 gnomAD v4
11g.118436553G>ACA382796844KMT2Ac.41G>A (p.Gly14Glu)
c.-798-32222G>A (n.-798-32222G>A)
c.214-11072G>A (n.214-11072G>A)
 gnomAD v4
11g.118436553G>CCA382796846KMT2Ac.41G>C (p.Gly14Ala)
c.-798-32222G>C (n.-798-32222G>C)
c.214-11072G>C (n.214-11072G>C)
11g.118436553G>TCA382796847KMT2Ac.41G>T (p.Gly14Val)
c.-798-32222G>T (n.-798-32222G>T)
c.214-11072G>T (n.214-11072G>T)
 gnomAD v4
11g.118436554G>ACA477086350KMT2Ac.42G>A (p.Gly14=)
c.-798-32221G>A (n.-798-32221G>A)
c.214-11071G>A (n.214-11071G>A)
 gnomAD v4
11g.118436554G>CCA477086353KMT2Ac.42G>C (p.Gly14=)
c.-798-32221G>C (n.-798-32221G>C)
c.214-11071G>C (n.214-11071G>C)
 dbSNP gnomAD v3 gnomAD v4
11g.118436554G=CA2003502128KMT2Ac.42G= (p.Gly14=)
c.-798-32221G= (n.-798-32221G=)
c.214-11071G= (n.214-11071G=)
11g.118436554G>TCA477086355KMT2Ac.42G>T (p.Gly14=)
c.-798-32221G>T (n.-798-32221G>T)
c.214-11071G>T (n.214-11071G>T)
 gnomAD v4
11g.118436555A>CCA382796855KMT2Ac.43A>C (p.Thr15Pro)
c.-798-32220A>C (n.-798-32220A>C)
c.214-11070A>C (n.214-11070A>C)
 dbSNP
11g.118436555A>GCA382796852KMT2Ac.43A>G (p.Thr15Ala)
c.-798-32220A>G (n.-798-32220A>G)
c.214-11070A>G (n.214-11070A>G)
 dbSNP
11g.118436555A>TCA382796849KMT2Ac.43A>T (p.Thr15Ser)
c.-798-32220A>T (n.-798-32220A>T)
c.214-11070A>T (n.214-11070A>T)
 gnomAD v4
11g.118436556C>ACA382796859KMT2Ac.44C>A (p.Thr15Asn)
c.-798-32219C>A (n.-798-32219C>A)
c.214-11069C>A (n.214-11069C>A)
 gnomAD v4
11g.118436556C>GCA382796857KMT2Ac.44C>G (p.Thr15Ser)
c.-798-32219C>G (n.-798-32219C>G)
c.214-11069C>G (n.214-11069C>G)
11g.118436556C>TCA382796862KMT2Ac.44C>T (p.Thr15Ile)
c.-798-32219C>T (n.-798-32219C>T)
c.214-11069C>T (n.214-11069C>T)
 gnomAD v4
11g.118436557C>ACA477086371KMT2Ac.45C>A (p.Thr15=)
c.-798-32218C>A (n.-798-32218C>A)
c.214-11068C>A (n.214-11068C>A)
 gnomAD v4
11g.118436557C>GCA477086372KMT2Ac.45C>G (p.Thr15=)
c.-798-32218C>G (n.-798-32218C>G)
c.214-11068C>G (n.214-11068C>G)
 gnomAD v4
11g.118436557C>TCA477086375KMT2Ac.45C>T (p.Thr15=)
c.-798-32218C>T (n.-798-32218C>T)
c.214-11068C>T (n.214-11068C>T)
 dbSNP gnomAD v3 gnomAD v4
11g.118436558A>CCA382796865KMT2Ac.46A>C (p.Thr16Pro)
c.-798-32217A>C (n.-798-32217A>C)
c.214-11067A>C (n.214-11067A>C)
 dbSNP gnomAD v4
11g.118436558A>GCA382796869KMT2Ac.46A>G (p.Thr16Ala)
c.-798-32217A>G (n.-798-32217A>G)
c.214-11067A>G (n.214-11067A>G)
 gnomAD v4
11g.118436558A>TCA382796867KMT2Ac.46A>T (p.Thr16Ser)
c.-798-32217A>T (n.-798-32217A>T)
c.214-11067A>T (n.214-11067A>T)
 gnomAD v4
11g.118436559C>ACA382796872KMT2Ac.47C>A (p.Thr16Asn)
c.-798-32216C>A (n.-798-32216C>A)
c.214-11066C>A (n.214-11066C>A)
 gnomAD v4
11g.118436559C>GCA382796874KMT2Ac.47C>G (p.Thr16Ser)
c.-798-32216C>G (n.-798-32216C>G)
c.214-11066C>G (n.214-11066C>G)
 gnomAD v4
11g.118436559C>TCA382796876KMT2Ac.47C>T (p.Thr16Ile)
c.-798-32216C>T (n.-798-32216C>T)
c.214-11066C>T (n.214-11066C>T)
 gnomAD v3 gnomAD v4
11g.118436560C>ACA477086391KMT2Ac.48C>A (p.Thr16=)
c.-798-32215C>A (n.-798-32215C>A)
c.214-11065C>A (n.214-11065C>A)
 gnomAD v4
11g.118436560C=CA2003502133KMT2Ac.48C= (p.Thr16=)
c.-798-32215C= (n.-798-32215C=)
c.214-11065C= (n.214-11065C=)
11g.118436560C>GCA477086393KMT2Ac.48C>G (p.Thr16=)
c.-798-32215C>G (n.-798-32215C>G)
c.214-11065C>G (n.214-11065C>G)
 dbSNP gnomAD v4
11g.118436560C>TCA477086395KMT2Ac.48C>T (p.Thr16=)
c.-798-32215C>T (n.-798-32215C>T)
c.214-11065C>T (n.214-11065C>T)
 ClinVar dbSNP gnomAD v4
11g.118436563_118436568delCA2616260569KMT2Ac.51_56del (p.Gly18_Gly19del)
c.-798-32212_-798-32207del (n.-798-32212_-798-32207del)
c.214-11062_214-11057del (n.214-11062_214-11057del)
 gnomAD v4
11g.118436561G>ACA382796879KMT2Ac.49G>A (p.Gly17Arg)
c.-798-32214G>A (n.-798-32214G>A)
c.214-11064G>A (n.214-11064G>A)
 gnomAD v4
11g.118436561G>CCA382796880KMT2Ac.49G>C (p.Gly17Arg)
c.-798-32214G>C (n.-798-32214G>C)
c.214-11064G>C (n.214-11064G>C)
 dbSNP gnomAD v4
11g.118436561G>TCA382796881KMT2Ac.49G>T (p.Gly17Trp)
c.-798-32214G>T (n.-798-32214G>T)
c.214-11064G>T (n.214-11064G>T)
 gnomAD v4
11g.118436565delCA2574995185KMT2Ac.53del (p.Gly18AlafsTer10)
c.-798-32210del (n.-798-32210del)
c.214-11060del (n.214-11060del)
 gnomAD v4
11g.118436568_118436600dupCA2725031454KMT2Ac.56_88dup (p.Gly29_Ala30insGlyGlyGlyGlyGlyArgArgGlyLeuGlyGly)
c.-798-32207_-798-32175dup (n.-798-32207_-798-32175dup)
c.214-11057_214-11025dup (n.214-11057_214-11025dup)
 dbSNP
11g.118436562G>ACA382796882KMT2Ac.50G>A (p.Gly17Glu)
c.-798-32213G>A (n.-798-32213G>A)
c.214-11063G>A (n.214-11063G>A)
 gnomAD v4
11g.118436562G>CCA382796883KMT2Ac.50G>C (p.Gly17Ala)
c.-798-32213G>C (n.-798-32213G>C)
c.214-11063G>C (n.214-11063G>C)
11g.118436562G>TCA382796884KMT2Ac.50G>T (p.Gly17Val)
c.-798-32213G>T (n.-798-32213G>T)
c.214-11063G>T (n.214-11063G>T)
 gnomAD v4
11g.118436563G>ACA477086413KMT2Ac.51G>A (p.Gly17=)
c.-798-32212G>A (n.-798-32212G>A)
c.214-11062G>A (n.214-11062G>A)
 dbSNP gnomAD v4
11g.118436563G>CCA477086415KMT2Ac.51G>C (p.Gly17=)
c.-798-32212G>C (n.-798-32212G>C)
c.214-11062G>C (n.214-11062G>C)
 gnomAD v4
11g.118436563G=CA2003502138KMT2Ac.51G= (p.Gly17=)
c.-798-32212G= (n.-798-32212G=)
c.214-11062G= (n.214-11062G=)
11g.118436563G>TCA477086417KMT2Ac.51G>T (p.Gly17=)
c.-798-32212G>T (n.-798-32212G>T)
c.214-11062G>T (n.214-11062G>T)
 gnomAD v4
11g.118436563_118436572delinsGGGCGGCGGCCA2003502140KMT2Ac.51_60delinsGGGCGGCGGC (p.Gly17=)
c.-798-32212_-798-32203delinsGGGCGGCGGC (n.-798-32212_-798-32203delinsGGGCGGCGGC)
c.214-11062_214-11053delinsGGGCGGCGGC (n.214-11062_214-11053delinsGGGCGGCGGC)
11g.118436564G>ACA382796885KMT2Ac.52G>A (p.Gly18Ser)
c.-798-32211G>A (n.-798-32211G>A)
c.214-11061G>A (n.214-11061G>A)
 gnomAD v4
11g.118436564G>CCA382796886KMT2Ac.52G>C (p.Gly18Arg)
c.-798-32211G>C (n.-798-32211G>C)
c.214-11061G>C (n.214-11061G>C)

Number of alleles fetched