ClinVar Miner

List of variants reported as likely benign for acute leukemia by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (47):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_002074.5(GNB1):c.462C>T (p.Asp154=) rs77027087 0.01689
NM_002520.7(NPM1):c.847-5T>C rs191111314 0.01680
NM_002520.7(NPM1):c.543T>C (p.Phe181=) rs61755048 0.00991
NM_002485.5(NBN):c.797C>T (p.Pro266Leu) rs769420 0.00955
NM_002485.5(NBN):c.2146A>G (p.Asn716Asp) rs72563785 0.00830
NM_002485.5(NBN):c.1489A>G (p.Thr497Ala) rs3026268 0.00711
NM_004327.4(BCR):c.606C>T (p.Ser202=) rs147507158 0.00655
NM_002485.5(NBN):c.1882G>A (p.Glu628Lys) rs115321485 0.00466
NM_006185.4(NUMA1):c.2937T>C (p.Asn979=) rs142372284 0.00416
NM_006185.4(NUMA1):c.5285G>A (p.Arg1762His) rs149588226 0.00414
NM_032638.5(GATA2):c.710G>A (p.Gly237Asp) rs191501191 0.00327
NM_002485.5(NBN):c.1222A>G (p.Lys408Glu) rs34120922 0.00276
NM_198253.3(TERT):c.1574-7G>A rs34846301 0.00220
NM_033360.4(KRAS):c.5-18A>G rs200189105 0.00100
NM_004972.4(JAK2):c.380G>A (p.Gly127Asp) rs56118985 0.00048
NM_198253.3(TERT):c.1932G>A (p.Thr644=) rs148582238 0.00031
NM_004985.5(KRAS):c.24A>G (p.Val8=) rs147406419 0.00025
NM_000222.3(KIT):c.2502G>A (p.Lys834=) rs146992614 0.00014
NM_033360.4(KRAS):c.90C>T (p.Asp30=) rs113623140 0.00011
NM_198253.3(TERT):c.2079C>T (p.Phe693=) rs371759577 0.00011
NM_002485.5(NBN):c.-2C>T rs202104448 0.00010
NM_033360.4(KRAS):c.4+5G>A rs201789109 0.00006
NM_000222.3(KIT):c.840G>C (p.Ala280=) rs142772432 0.00004
NM_001754.5(RUNX1):c.1338C>T (p.Leu446=) rs769628054 0.00004
NM_004985.5(KRAS):c.451-5652C>T rs727505314 0.00004
NM_198253.3(TERT):c.2190C>T (p.Ala730=) rs138128892 0.00003
NM_002485.5(NBN):c.995-17A>G rs372875251 0.00002
NM_000222.3(KIT):c.531C>T (p.Arg177=) rs756722358 0.00001
NM_198253.3(TERT):c.3303G>A (p.Thr1101=) rs551516320 0.00001
NM_198253.3(TERT):c.375C>T (p.Asn125=) rs1751256209 0.00001
NM_001754.5(RUNX1):c.1272G>C (p.Ser424=) rs1459260782
NM_002485.5(NBN):c.540C>T (p.Phe180=) rs1060504928
NM_004985.5(KRAS):c.112-9C>T rs727504298
NM_198253.3(TERT):c.1110C>G (p.Pro370=) rs1579597009

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