ClinVar Miner

List of variants in gene XIAP reported as uncertain significance for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP
NC_000023.11:g.(?_123885637)_(123886559_?)dup
NC_000023.11:g.(?_123885637)_(123907201_?)dup
NM_001167.3(XIAP):c.*1940T>C rs755490620
NM_001167.3(XIAP):c.*2401C>T rs771727226
NM_001167.3(XIAP):c.*2521A>G rs746553843
NM_001167.3(XIAP):c.*253C>T rs1057515749
NM_001167.3(XIAP):c.*3201A>G rs1057515752
NM_001167.3(XIAP):c.*3205T>C rs777738703
NM_001167.3(XIAP):c.*3573G>A rs1037858715
NM_001167.3(XIAP):c.*3997A>G rs1057515755
NM_001167.3(XIAP):c.*6211C>T rs1022688672
NM_001167.3(XIAP):c.*6216G>A rs1057515760
NM_001167.3(XIAP):c.*6220C>T rs370656891
NM_001167.3(XIAP):c.*6221G>A rs757596272
NM_001167.3(XIAP):c.*870G>C rs185823003
NM_001167.3(XIAP):c.171A>G (p.Glu57=) rs1556404487
NM_001167.3(XIAP):c.435G>T (p.Gln145His) rs759909620
NM_001167.3(XIAP):c.562G>A (p.Gly188Arg) rs1602544454
NM_001167.3(XIAP):c.683T>G (p.Phe228Cys) rs140973844
NM_001167.3(XIAP):c.844G>A (p.Glu282Lys) rs777303823
NM_001167.3(XIAP):c.978-10_978-4del rs1602549230
NM_001167.3(XIAP):c.978-9A>G rs1602549234
NM_001167.4(XIAP):c.*1481C>T
NM_001167.4(XIAP):c.*1705A>G
NM_001167.4(XIAP):c.*1869G>A
NM_001167.4(XIAP):c.*1904G>A
NM_001167.4(XIAP):c.*1950C>T
NM_001167.4(XIAP):c.*2488C>T
NM_001167.4(XIAP):c.*3408G>T
NM_001167.4(XIAP):c.*3544G>A
NM_001167.4(XIAP):c.*3547C>G
NM_001167.4(XIAP):c.*3589A>C
NM_001167.4(XIAP):c.*3673C>T
NM_001167.4(XIAP):c.*3845A>G
NM_001167.4(XIAP):c.*4336T>G
NM_001167.4(XIAP):c.*4691G>A
NM_001167.4(XIAP):c.*5986G>A
NM_001167.4(XIAP):c.*6009C>T
NM_001167.4(XIAP):c.*6010G>A
NM_001167.4(XIAP):c.*6256T>C
NM_001167.4(XIAP):c.*866A>G
NM_001167.4(XIAP):c.*93T>G
NM_001167.4(XIAP):c.-142G>C
NM_001167.4(XIAP):c.1045_1047GAG[1] (p.Glu350del) rs199683465
NM_001167.4(XIAP):c.1048G>A (p.Glu350Lys)
NM_001167.4(XIAP):c.1058T>C (p.Val353Ala)
NM_001167.4(XIAP):c.1154G>A (p.Ser385Asn)
NM_001167.4(XIAP):c.1237G>A (p.Asp413Asn)
NM_001167.4(XIAP):c.1317G>C (p.Glu439Asp)
NM_001167.4(XIAP):c.1327C>T (p.Arg443Cys)
NM_001167.4(XIAP):c.416A>G (p.Tyr139Cys)
NM_001167.4(XIAP):c.482A>G (p.Tyr161Cys)
NM_001167.4(XIAP):c.632A>G (p.Glu211Gly)
NM_001167.4(XIAP):c.838A>C (p.Asn280His)
NM_001167.4(XIAP):c.840C>G (p.Asn280Lys)
NM_001167.4(XIAP):c.844G>C (p.Glu282Gln)
NM_001167.4(XIAP):c.919C>A (p.Leu307Ile)

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