ClinVar Miner

List of variants reported as likely benign for acute myeloid leukemia by Invitae

Included ClinVar conditions (22):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_004364.4(CEBPA):c.111G>C (p.Ala37=) rs1323312485
NM_004364.4(CEBPA):c.120G>T (p.Ala40=) rs1555742292
NM_004364.4(CEBPA):c.129C>A (p.Pro43=) rs1060504476
NM_004364.4(CEBPA):c.132C>T (p.Ala44=) rs1060504474
NM_004364.4(CEBPA):c.138T>A (p.Pro46=) rs1387400759
NM_004364.4(CEBPA):c.153G>T (p.Pro51=) rs1054442664
NM_004364.4(CEBPA):c.159C>T (p.Gly53=) rs1555742279
NM_004364.4(CEBPA):c.174C>T (p.His58=) rs878854699
NM_004364.4(CEBPA):c.180G>T (p.Thr60=) rs1243562179
NM_004364.4(CEBPA):c.210G>A (p.Pro70=) rs1432277634
NM_004364.4(CEBPA):c.27G>A (p.Ala9=) rs1555742328
NM_004364.4(CEBPA):c.311_313dupGCG (p.Gly104_Asp105insGly) rs780345232
NM_004364.4(CEBPA):c.318T>C (p.Phe106=) rs1555742225
NM_004364.4(CEBPA):c.387C>G (p.Pro129=) rs1060504477
NM_004364.4(CEBPA):c.396C>T (p.Gly132=) rs1060504475
NM_004364.4(CEBPA):c.459G>A (p.Pro153=) rs779373951
NM_004364.4(CEBPA):c.501G>A (p.Glu167=) rs1277875501
NM_004364.4(CEBPA):c.522G>A (p.Ala174=) rs1272249243
NM_004364.4(CEBPA):c.558G>A (p.Pro186=) rs1338027134
NM_004364.4(CEBPA):c.561G>C (p.Pro187=) rs538441046
NM_004364.4(CEBPA):c.576G>A (p.Pro192=) rs878854703
NM_004364.4(CEBPA):c.576G>T (p.Pro192=) rs878854703
NM_004364.4(CEBPA):c.603G>A (p.Leu201=) rs1555742086
NM_004364.4(CEBPA):c.633G>T (p.Ala211=) rs1345901618
NM_004364.4(CEBPA):c.642C>T (p.Gly214=) rs1301372441
NM_004364.4(CEBPA):c.684G>A (p.Pro228=) rs1199384366
NM_004364.4(CEBPA):c.696G>T (p.Val232=) rs1213133617
NM_004364.4(CEBPA):c.762G>A (p.Lys254=) rs1366451304
NM_004364.4(CEBPA):c.789C>T (p.Leu263=) rs552131738
NM_004364.4(CEBPA):c.882C>T (p.Ile294=) rs376093748
NM_004364.4(CEBPA):c.888G>A (p.Val296=) rs772999335
NM_004364.4(CEBPA):c.942G>T (p.Val314=) rs377329266

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