ClinVar Miner

List of variants studied for central nervous system neoplasm by Institute of Human Genetics, University of Leipzig Medical Center

Included ClinVar conditions (109):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_004168.4(SDHA):c.91C>T (p.Arg31Ter) rs142441643 0.00025
NM_003001.5(SDHC):c.377A>G (p.Tyr126Cys) rs898854295 0.00003
NM_017841.4(SDHAF2):c.352A>G (p.Ile118Val) rs747994812 0.00001
NM_003002.4(SDHD):c.217dup (p.Ser73fs) rs2135269358
NM_003072.5(SMARCA4):c.3440_3441del (p.Gly1146_Ser1147insTer)
NM_017841.4(SDHAF2):c.42_45del (p.Ala15fs) rs1862009020

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