List of variants in gene combination LOC129929542, SDHB reported as uncertain significance for benign neoplasm of adrenal gland

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
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.58G>C (p.Gly20Arg)	rs1557749649	0.00001
NM_003000.3(SDHB):c.61G>A (p.Ala21Thr)	rs774266782	0.00001
NC_000001.10:g.(?_17359545)_(17380524_?)dup
NC_000001.10:g.(?_17371246)_(17380524_?)dup
NM_003000.3(SDHB):c.50C>A (p.Thr17Asn)	rs138979875
NM_003000.3(SDHB):c.50C>G (p.Thr17Ser)
NM_003000.3(SDHB):c.52C>T (p.Leu18Phe)	rs2101551686
NM_003000.3(SDHB):c.58G>A (p.Gly20Arg)
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.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.68T>C (p.Leu23Pro)
NM_003000.3(SDHB):c.70C>A (p.Gln24Lys)
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.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+6T>G
NM_003000.3(SDHB):c.72G>A (p.Gln24=)	rs1553179312
NM_003000.3(SDHB):c.72G>C (p.Gln24His)	rs1553179312

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