ClinVar Miner

List of variants in gene RPS26 reported as likely benign for aplastic anemia

Included ClinVar conditions (98):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_001029.5(RPS26):c.-3A>G rs181174349 0.00056
NM_001029.5(RPS26):c.63T>A (p.Ile21=) rs148167449 0.00008
NM_001029.5(RPS26):c.-33C>T rs372794158 0.00006
NM_001029.5(RPS26):c.60T>A (p.Pro20=) rs368838700 0.00005
NM_001029.5(RPS26):c.270A>G (p.Glu90=) rs139056836 0.00004
NM_001029.5(RPS26):c.181+10T>G rs201191387 0.00003
NM_001029.5(RPS26):c.207G>C (p.Val69=) rs776240183 0.00002
NM_001029.5(RPS26):c.291C>T (p.Pro97=) rs766621663 0.00001
NM_001029.5(RPS26):c.3+14C>T rs763770729 0.00001
NM_001029.5(RPS26):c.3+20G>C rs759864837 0.00001
NM_001029.5(RPS26):c.315T>A (p.Gly105=) rs554297156 0.00001
NM_001029.5(RPS26):c.42C>T (p.Gly14=) rs771196681 0.00001
NM_001029.5(RPS26):c.69C>T (p.Cys23=) rs986563758 0.00001
NM_001029.5(RPS26):c.81C>T (p.Ala27=) rs773982358 0.00001
NM_001029.5(RPS26):c.93C>T (p.Pro31=) rs760255764 0.00001
NM_001029.5(RPS26):c.-27C>T rs200831849
NM_001029.5(RPS26):c.-31C>T rs17118262
NM_001029.5(RPS26):c.-9G>T rs372708429
NM_001029.5(RPS26):c.120C>A (p.Val40=)
NM_001029.5(RPS26):c.120C>G (p.Val40=)
NM_001029.5(RPS26):c.129C>T (p.Asn43=)
NM_001029.5(RPS26):c.144A>G (p.Ala48=) rs150715896
NM_001029.5(RPS26):c.144A>T (p.Ala48=)
NM_001029.5(RPS26):c.181+19C>G rs201040758
NM_001029.5(RPS26):c.181+8G>C
NM_001029.5(RPS26):c.182-16_182-15del
NM_001029.5(RPS26):c.182-20C>T
NM_001029.5(RPS26):c.182-9A>G
NM_001029.5(RPS26):c.183C>G (p.Ala61=)
NM_001029.5(RPS26):c.201G>A (p.Leu67=) rs1371451613
NM_001029.5(RPS26):c.213A>G (p.Leu71=)
NM_001029.5(RPS26):c.288A>G (p.Thr96=)
NM_001029.5(RPS26):c.3+10C>T
NM_001029.5(RPS26):c.3+12T>C
NM_001029.5(RPS26):c.3+13G>T rs199917474
NM_001029.5(RPS26):c.3+14C>A
NM_001029.5(RPS26):c.3+14C>G rs763770729
NM_001029.5(RPS26):c.3+7C>G rs115750993
NM_001029.5(RPS26):c.3+7C>T rs115750993
NM_001029.5(RPS26):c.3+9T>A rs545595719
NM_001029.5(RPS26):c.312+7A>G
NM_001029.5(RPS26):c.313-10dup
NM_001029.5(RPS26):c.313-17_313-14del rs771654280
NM_001029.5(RPS26):c.313-7C>T
NM_001029.5(RPS26):c.327T>C (p.Arg109=) rs56696262
NM_001029.5(RPS26):c.333A>T (p.Pro111=) rs1179423823
NM_001029.5(RPS26):c.336A>G (p.Pro112=)
NM_001029.5(RPS26):c.4-10C>T
NM_001029.5(RPS26):c.4-13C>T rs962158538
NM_001029.5(RPS26):c.4-4G>T rs2136753773
NM_001029.5(RPS26):c.4-7G>C rs1288899882
NM_001029.5(RPS26):c.93C>G (p.Pro31=)

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