ClinVar Miner

List of variants in gene combination LOC129929542, SDHB reported as likely benign for nervous system cancer

Included ClinVar conditions (69):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_003000.3(SDHB):c.65G>C (p.Cys22Ser) rs141230910 0.00057
NM_003000.3(SDHB):c.66C>T (p.Cys22=) rs772853861 0.00002
NM_003000.3(SDHB):c.51C>A (p.Thr17=) rs550555402 0.00001
NM_003000.3(SDHB):c.72+18A>G rs758905319 0.00001
NM_003000.3(SDHB):c.51C>G (p.Thr17=)
NM_003000.3(SDHB):c.51C>T (p.Thr17=) rs550555402
NM_003000.3(SDHB):c.54T>C (p.Leu18=) rs759446168
NM_003000.3(SDHB):c.54T>G (p.Leu18=) rs759446168
NM_003000.3(SDHB):c.57C>T (p.Gly19=) rs1326601709
NM_003000.3(SDHB):c.60A>C (p.Gly20=)
NM_003000.3(SDHB):c.63C>G (p.Ala21=) rs1557749647
NM_003000.3(SDHB):c.67C>T (p.Leu23=)
NM_003000.3(SDHB):c.69G>C (p.Leu23=)
NM_003000.3(SDHB):c.72+10G>A rs2101551608
NM_003000.3(SDHB):c.72+10G>C rs2101551608
NM_003000.3(SDHB):c.72+13G>T
NM_003000.3(SDHB):c.72+14C>T rs1321607765
NM_003000.3(SDHB):c.72+15C>T
NM_003000.3(SDHB):c.72+17C>G rs1031878905
NM_003000.3(SDHB):c.72+18A>C
NM_003000.3(SDHB):c.72+19G>C rs1466555262
NM_003000.3(SDHB):c.72+7C>A rs1553179311
NM_003000.3(SDHB):c.72+7C>G
NM_003000.3(SDHB):c.72+7C>T rs1553179311
NM_003000.3(SDHB):c.72+8C>G rs1570963404
NM_003000.3(SDHB):c.72+8C>T rs1570963404

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