ClinVar Miner

List of variants in gene IL10RA reported as pathogenic for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_001558.4(IL10RA):c.784C>T (p.Arg262Cys) rs149491038 0.00003
NM_001558.4(IL10RA):c.251C>T (p.Thr84Ile) rs137853580 0.00001
NM_001558.4(IL10RA):c.421G>A (p.Gly141Arg) rs137853579 0.00001
NM_001558.4(IL10RA):c.537G>A (p.Thr179=) rs1419560997 0.00001
NM_001558.4(IL10RA):c.634C>T (p.Arg212Ter) rs1591263883 0.00001
NM_001558.4(IL10RA):c.258_279dup (p.Asn94fs)
NM_001558.4(IL10RA):c.301C>T (p.Arg101Trp) rs368287711
NM_001558.4(IL10RA):c.349C>T (p.Arg117Cys)
NM_001558.4(IL10RA):c.439_452del (p.Arg147fs)
NM_001558.4(IL10RA):c.470A>G (p.Tyr157Cys)
NM_001558.4(IL10RA):c.501T>G (p.Tyr167Ter)
NM_001558.4(IL10RA):c.618dup (p.Pro207fs) rs1187971271
NM_001558.4(IL10RA):c.756C>A (p.Tyr252Ter) rs2134991615
NM_001558.4(IL10RA):c.769C>T (p.Gln257Ter) rs1214626558

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