ClinVar Miner

List of variants in gene IL1RAPL1 reported as uncertain significance for X-linked disease

Included ClinVar conditions (311):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_014271.4(IL1RAPL1):c.-302dup rs779869307
NM_014271.4(IL1RAPL1):c.-303_-302del rs779869307
NM_014271.4(IL1RAPL1):c.-402G>A rs1057515846
NM_014271.4(IL1RAPL1):c.-405T>A rs762456633
NM_014271.4(IL1RAPL1):c.-82C>A rs1057515849
NM_014271.4(IL1RAPL1):c.1368T>A (p.Thr456=) rs1057515851
NM_014271.4(IL1RAPL1):c.1602G>A (p.Leu534=)
NM_014271.4(IL1RAPL1):c.1690A>C (p.Ile564Leu) rs1057515852
NM_014271.4(IL1RAPL1):c.1910C>G (p.Thr637Ser)
NM_014271.4(IL1RAPL1):c.206G>A (p.Ser69Asn) rs747458852
NM_014271.4(IL1RAPL1):c.408T>C (p.Gly136=)
NM_014271.4(IL1RAPL1):c.424C>G (p.Leu142Val) rs765477668
NM_014271.4(IL1RAPL1):c.779G>A (p.Gly260Asp)
NM_014271.4(IL1RAPL1):c.83-8dup rs773751585

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