ClinVar Miner

Variants in gene IL10RA with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 11
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HGVS dbSNP gnomAD frequency
NM_001558.4(IL10RA):c.181C>G (p.Leu61Val) rs4252250 0.01376
NM_001558.4(IL10RA):c.337G>A (p.Val113Ile) rs4252303 0.00655
NM_001558.4(IL10RA):c.21G>C (p.Val7=) rs4252301 0.00575
NM_001558.4(IL10RA):c.1188G>A (p.Arg396=) rs35465632 0.00388
NM_001558.4(IL10RA):c.75G>T (p.Glu25Asp) rs150140303 0.00324
NM_001558.4(IL10RA):c.67+8T>C rs200992970 0.00290
NM_001558.4(IL10RA):c.696C>T (p.Thr232=) rs4252311 0.00274
NM_001558.4(IL10RA):c.144C>T (p.Ile48=) rs140466541 0.00178
NM_001558.4(IL10RA):c.810+10G>A rs12290349 0.00092
NM_001558.4(IL10RA):c.1360G>A (p.Glu454Lys) rs79887053 0.00007
NM_001558.4(IL10RA):c.716T>C (p.Phe239Ser) rs541386535 0.00001

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