ClinVar Miner

List of variants in gene RNF135 studied for autosomal anomaly

Included ClinVar conditions (123):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_032322.4(RNF135):c.857G>A (p.Arg286His) rs121918162 0.00011
NM_032322.4(RNF135):c.727C>T (p.Gln243Ter) rs121918161 0.00003
NM_032322.4(RNF135):c.575C>T (p.Thr192Ile) rs1907708509 0.00001
NM_032322.4(RNF135):c.1015del (p.Val339fs) rs724159978
NM_032322.4(RNF135):c.742del (p.Leu248fs) rs724159977
Single allele

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