List of variants in gene LOC126861339, SDHD studied 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
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_003002.4(SDHD):c.34G>A (p.Gly12Ser)	rs34677591	0.00706
NC_000011.10:g.(?_112086898)_(112094980_?)del
NC_000011.9:g.(?_111957622)_(111965704_?)dup
NM_003002.3(SDHD):c.-84_*831del
NM_003002.4(SDHD):c.10dup (p.Leu4fs)	rs878854589
NM_003002.4(SDHD):c.13_14del (p.Trp5fs)	rs1566690018
NM_003002.4(SDHD):c.14G>A (p.Trp5Ter)	rs104894310
NM_003002.4(SDHD):c.18_21del (p.Leu7fs)	rs1555186662
NM_003002.4(SDHD):c.1A>G (p.Met1Val)	rs104894307
NM_003002.4(SDHD):c.33C>A (p.Cys11Ter)	rs104894309
NM_003002.4(SDHD):c.3G>C (p.Met1Ile)	rs80338842
NM_003002.4(SDHD):c.49C>T (p.Arg17Ter)	rs1314133983
NM_003002.4(SDHD):c.52+2T>G	rs587776644

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