ClinVar Miner

List of variants reported as other for central nervous system neoplasm by Donald Williams Parsons Laboratory, Baylor College of Medicine

Included ClinVar conditions (104):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001256071.3(RNF213):c.12841C>T (p.Arg4281Trp) rs765980348 0.00003
NM_002734.5(PRKAR1A):c.329C>T (p.Ala110Val) rs1194755479 0.00002
NM_000268.4(NF2):c.575A>G (p.Tyr192Cys) rs1555993319
NM_001123385.2(BCOR):c.3883_3884del (p.Leu1296fs) rs886042842
NM_001356.5(DDX3X):c.1033G>C (p.Val345Leu) rs1555953796
NM_001356.5(DDX3X):c.1588G>T (p.Gly530Cys) rs1555954272
NM_001356.5(DDX3X):c.1592G>A (p.Arg531His) rs1555954275
NM_001374828.1(ARID1B):c.3714+1G>A rs1554231278
NM_001455.4(FOXO3):c.583A>T (p.Lys195Ter) rs1554209779
NM_001455.4(FOXO3):c.699G>A (p.Trp233Ter) rs1554218944
NM_001904.4(CTNNB1):c.101G>A (p.Gly34Glu) rs28931589
NM_001904.4(CTNNB1):c.94G>T (p.Asp32Tyr) rs28931588
NM_001904.4(CTNNB1):c.98C>G (p.Ser33Cys) rs121913400
NM_002107.7(H3-3A):c.103G>A (p.Gly35Arg) rs1553260624
NM_003072.5(SMARCA4):c.2729C>T (p.Thr910Met) rs1238758086
NM_005120.3(MED12):c.5980C>T (p.Arg1994Trp) rs1556339256
NM_006015.6(ARID1A):c.2732G>T (p.Arg911Met) rs1553152166
NM_007363.5(NONO):c.731dup (p.Asn244fs) rs1555950011
NM_022455.5(NSD1):c.7147G>T (p.Gly2383Cys) rs1554207664

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