ClinVar Miner

List of variants in gene combination IQCG, RPL35A 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: 42
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HGVS dbSNP gnomAD frequency
NM_000996.4(RPL35A):c.*14C>A rs10022 0.00200
NM_000996.4(RPL35A):c.165-16C>A rs373782117 0.00041
NM_000996.4(RPL35A):c.12-18G>A rs373448841 0.00007
NM_000996.4(RPL35A):c.21C>T (p.Ser7=) rs145660527 0.00006
NM_000996.4(RPL35A):c.12-5C>G rs541454864 0.00005
NM_000996.4(RPL35A):c.184G>T (p.Gly62Cys) rs146882967 0.00003
NM_000996.4(RPL35A):c.327G>A (p.Arg109=) rs754407977 0.00003
NM_000996.4(RPL35A):c.164+18G>A rs749642279 0.00002
NM_000996.4(RPL35A):c.11+11T>C rs766619628 0.00001
NM_000996.4(RPL35A):c.11+17T>C rs780298603 0.00001
NM_000996.4(RPL35A):c.12-13T>A rs778146996 0.00001
NM_000996.4(RPL35A):c.141C>T (p.Cys47=) rs1440792535 0.00001
NM_000996.4(RPL35A):c.57G>A (p.Arg19=) rs769775044 0.00001
NM_000996.4(RPL35A):c.*21T>A rs199693579
NM_000996.4(RPL35A):c.105C>T (p.Ala35=)
NM_000996.4(RPL35A):c.12-18G>T
NM_000996.4(RPL35A):c.12-4T>G
NM_000996.4(RPL35A):c.12-5C>T
NM_000996.4(RPL35A):c.12-7G>T rs2109804559
NM_000996.4(RPL35A):c.147T>C (p.Tyr49=)
NM_000996.4(RPL35A):c.164+13C>T rs2109805109
NM_000996.4(RPL35A):c.164+15C>G rs890177445
NM_000996.4(RPL35A):c.164+15C>T
NM_000996.4(RPL35A):c.165-15C>G
NM_000996.4(RPL35A):c.165-20C>T
NM_000996.4(RPL35A):c.183C>T (p.Gly61=) rs370212853
NM_000996.4(RPL35A):c.186C>T (p.Gly62=)
NM_000996.4(RPL35A):c.204A>G (p.Arg68=)
NM_000996.4(RPL35A):c.258C>A (p.Ala86=)
NM_000996.4(RPL35A):c.282T>C (p.Ala94=) rs201018840
NM_000996.4(RPL35A):c.282T>G (p.Ala94=)
NM_000996.4(RPL35A):c.306A>C (p.Arg102=)
NM_000996.4(RPL35A):c.309+7A>G
NM_000996.4(RPL35A):c.310-20G>A rs200360699
NM_000996.4(RPL35A):c.310-20G>C rs200360699
NM_000996.4(RPL35A):c.310-6del rs2109818917
NM_000996.4(RPL35A):c.321C>T (p.Pro107=)
NM_000996.4(RPL35A):c.324A>G (p.Ser108=) rs751160471
NM_000996.4(RPL35A):c.332A>G (p.Ter111=)
NM_000996.4(RPL35A):c.33T>C (p.Phe11=) rs751752645
NM_000996.4(RPL35A):c.75A>G (p.Thr25=) rs1244935223
NM_000996.4(RPL35A):c.90T>C (p.Ile30=) rs2109804838

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