ClinVar Miner

List of variants in gene combination RPS10, RPS10-NUDT3 reported as likely benign for anemia (disease)

Included ClinVar conditions (262):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_001014.4(RPS10):c.-43T>G rs111597547
NM_001014.4(RPS10):c.-47A>G rs529023165
NM_001014.4(RPS10):c.150+9delG rs372641476
NM_001014.5(RPS10):c.*43A>G rs200231286
NM_001014.5(RPS10):c.-14C>T rs576997899
NM_001014.5(RPS10):c.-21C>G rs181470609
NM_001014.5(RPS10):c.-29C>T rs140822093
NM_001014.5(RPS10):c.1-3C>G rs375500787
NM_001014.5(RPS10):c.111C>G (p.Asp37Glu) rs374314919
NM_001014.5(RPS10):c.135C>T (p.Val45=) rs148901210
NM_001014.5(RPS10):c.204C>T (p.Tyr68=) rs368563040
NM_001014.5(RPS10):c.231G>A (p.Gln77=) rs147863199
NM_001014.5(RPS10):c.408C>T (p.Ala136=) rs147566753
NM_001014.5(RPS10):c.6G>A (p.Leu2=) rs146246722
NM_001014.5(RPS10):c.71A>G (p.Lys24Arg) rs201147592

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