List of variants in gene SDHC reported as likely pathogenic for central nervous system neoplasm

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.377A>G (p.Tyr126Cys)	rs898854295	0.00003
NM_003001.5(SDHC):c.148C>T (p.Arg50Cys)	rs587778661	0.00001
NC_000001.10:g.(?_161310384)_(161310445_?)dup
NC_000001.10:g.(?_161326457)_(161326640_?)dup
NC_000001.11:g.(?_161340584)_(161340665_?)dup
NM_003001.5(SDHC):c.160C>A (p.Pro54Thr)	rs1553262444
NM_003001.5(SDHC):c.171_179+15del	rs1671156558
NM_003001.5(SDHC):c.179+1G>C	rs1057517818
NM_003001.5(SDHC):c.179+1G>T	rs1057517818
NM_003001.5(SDHC):c.179+2T>A
NM_003001.5(SDHC):c.180-2A>G	rs1363265634
NM_003001.5(SDHC):c.20+1G>A
NM_003001.5(SDHC):c.20+1G>T	rs1249046874
NM_003001.5(SDHC):c.224G>A (p.Gly75Asp)	rs786205147
NM_003001.5(SDHC):c.2T>G (p.Met1Arg)	rs1670517782
NM_003001.5(SDHC):c.379C>A (p.His127Asn)	rs1485675090
NM_003001.5(SDHC):c.379C>G (p.His127Asp)	rs1485675090
NM_003001.5(SDHC):c.405+1del	rs1558182956
NM_003001.5(SDHC):c.406-1G>A
NM_003001.5(SDHC):c.422_423insT (p.Lys141fs)	rs1672548902
NM_003001.5(SDHC):c.77+1G>A	rs1558164647
NM_003001.5(SDHC):c.77+1G>C
NM_003001.5(SDHC):c.78-1G>T	rs786202200
NM_003001.5(SDHC):c.78-2A>G

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