ClinVar Miner

List of variants reported as uncertain significance for acute myeloid leukemia by Clinical Genomics Lab,St. Jude Children's Research Hospital

Included ClinVar conditions (22):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_000038.6(APC):c.319T>G (p.Ser107Ala) rs1485866385
NM_000059.3(BRCA2):c.5747A>G (p.His1916Arg) rs431825334
NM_000059.3(BRCA2):c.6560C>T (p.Pro2187Leu) rs56019712
NM_000059.3(BRCA2):c.8611G>C (p.Glu2871Gln) rs587782860
NM_000251.2(MSH2):c.1156G>A (p.Asp386Asn) rs1419725521
NM_000251.2(MSH2):c.1511-13_1511-9delinsGT rs1558510749
NM_000267.3(NF1):c.1588G>A (p.Val530Ile) rs145191978
NM_000267.3(NF1):c.2747A>G (p.Asn916Ser) rs765043916
NM_000368.4(TSC1):c.3439A>G (p.Ser1147Gly) rs768624733
NM_000455.4(STK11):c.970C>G (p.Pro324Ala) rs549474196
NM_000548.5(TSC2):c.5336A>G (p.Gln1779Arg) rs748947919
NM_001083602.2(PTCH1):c.1861G>A (p.Val621Met) rs374691153
NM_004304.5(ALK):c.1283-5T>C rs377214413
NM_004360.5(CDH1):c.1955T>G (p.Leu652Trp) rs1567513174
NM_005633.3(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_007373.3(SHOC2):c.1741A>G (p.Met581Val) rs1470655019
NM_016734.3(PAX5):c.701T>C (p.Leu234Pro) rs753068558
NM_017849.3(TMEM127):c.121A>G (p.Ile41Val) rs760633411
NM_017849.3(TMEM127):c.31G>T (p.Gly11Cys)
NM_177438.2(DICER1):c.2720T>C (p.Ile907Thr) rs200408568
NM_177438.2(DICER1):c.3553G>A (p.Ala1185Thr) rs150514959

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