ClinVar Miner

List of variants in gene LOC129929542, SDHB studied for small intestine neoplasm

Included ClinVar conditions (17):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
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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.49A>G (p.Thr17Ala) rs1060503756 0.00001
NM_003000.3(SDHB):c.50C>T (p.Thr17Ile) rs138979875 0.00001
NM_003000.3(SDHB):c.51C>A (p.Thr17=) rs550555402 0.00001
NM_003000.3(SDHB):c.58G>C (p.Gly20Arg) rs1557749649 0.00001
NM_003000.3(SDHB):c.61G>A (p.Ala21Thr) rs774266782 0.00001
NM_003000.3(SDHB):c.72+18A>G rs758905319 0.00001
NC_000001.10:g.(?_17359545)_(17380524_?)dup
NC_000001.10:g.(?_17371246)_(17380524_?)dup
NC_000001.11:g.(?_17053938)_(17054029_?)del
NM_003000.3(SDHB):c.50C>A (p.Thr17Asn) rs138979875
NM_003000.3(SDHB):c.50C>G (p.Thr17Ser)
NM_003000.3(SDHB):c.51C>G (p.Thr17=)
NM_003000.3(SDHB):c.51C>T (p.Thr17=) rs550555402
NM_003000.3(SDHB):c.52C>T (p.Leu18Phe) rs2101551686
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.58G>A (p.Gly20Arg)
NM_003000.3(SDHB):c.60A>C (p.Gly20=)
NM_003000.3(SDHB):c.61G>T (p.Ala21Ser)
NM_003000.3(SDHB):c.62C>G (p.Ala21Gly) rs2078163173
NM_003000.3(SDHB):c.62C>T (p.Ala21Val) rs2078163173
NM_003000.3(SDHB):c.63C>G (p.Ala21=) rs1557749647
NM_003000.3(SDHB):c.63dup (p.Cys22fs) rs1570963451
NM_003000.3(SDHB):c.65G>A (p.Cys22Tyr) rs141230910
NM_003000.3(SDHB):c.65G>T (p.Cys22Phe) rs141230910
NM_003000.3(SDHB):c.67C>G (p.Leu23Val) rs1553179319
NM_003000.3(SDHB):c.67C>T (p.Leu23=)
NM_003000.3(SDHB):c.68T>C (p.Leu23Pro)
NM_003000.3(SDHB):c.69G>C (p.Leu23=)
NM_003000.3(SDHB):c.70C>T (p.Gln24Ter) rs1570963430
NM_003000.3(SDHB):c.71A>C (p.Gln24Pro) rs878854580
NM_003000.3(SDHB):c.71A>G (p.Gln24Arg) rs878854580
NM_003000.3(SDHB):c.71A>T (p.Gln24Leu)
NM_003000.3(SDHB):c.71_72delinsCC (p.Gln24Pro) rs2078163018
NM_003000.3(SDHB):c.71dup (p.Ala25fs) rs1131691057
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+1G>A rs587782703
NM_003000.3(SDHB):c.72+1G>T rs587782703
NM_003000.3(SDHB):c.72+3G>A rs569245129
NM_003000.3(SDHB):c.72+3G>C
NM_003000.3(SDHB):c.72+4A>G rs1228108598
NM_003000.3(SDHB):c.72+5G>A rs878854581
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
NM_003000.3(SDHB):c.72G>A (p.Gln24=) rs1553179312
NM_003000.3(SDHB):c.72G>C (p.Gln24His) rs1553179312

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