ClinVar Miner

List of variants in gene LOC107985033, SLFN14 studied for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_001129820.2(SLFN14):c.1153A>G (p.Lys385Glu) rs321612 0.64723
NM_001129820.2(SLFN14):c.1066C>T (p.Pro356Ser) rs321613 0.64716
NM_001129820.2(SLFN14):c.1061-11T>C rs321614 0.46920
NM_001129820.2(SLFN14):c.1348A>G (p.Lys450Glu) rs79007502 0.02530
NM_001129820.2(SLFN14):c.1356G>T (p.Gln452His) rs572233110 0.00001
NM_001129820.2(SLFN14):c.1108G>A (p.Ala370Thr) rs989179732
NM_001129820.2(SLFN14):c.1382T>A (p.Ile461Lys)

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