List of variants in gene SDHD reported as likely pathogenic for adrenal gland 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: 26

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HGVS	dbSNP	gnomAD frequency
NM_003002.4(SDHD):c.53-1G>T	rs1291507545	0.00001
NM_003002.4(SDHD):c.117del (p.Ile40fs)
NM_003002.4(SDHD):c.128G>A (p.Trp43Ter)	rs2135267337
NM_003002.4(SDHD):c.147dup (p.His50fs)	rs876659130
NM_003002.4(SDHD):c.148C>G (p.His50Asp)	rs779249550
NM_003002.4(SDHD):c.197_198delinsAA (p.Trp66Ter)
NM_003002.4(SDHD):c.217dup (p.Ser73fs)	rs2135269358
NM_003002.4(SDHD):c.275A>T (p.Asp92Val)	rs786205436
NM_003002.4(SDHD):c.298del (p.Thr100fs)	rs1555187067
NM_003002.4(SDHD):c.304C>A (p.His102Asn)	rs786202403
NM_003002.4(SDHD):c.304C>T (p.His102Tyr)	rs786202403
NM_003002.4(SDHD):c.305A>C (p.His102Pro)	rs104894302
NM_003002.4(SDHD):c.315-1G>A	rs1555187566
NM_003002.4(SDHD):c.320T>G (p.Leu107Arg)	rs876658477
NM_003002.4(SDHD):c.340T>C (p.Tyr114His)	rs876659276
NM_003002.4(SDHD):c.361C>T (p.Gln121Ter)	rs878854594
NM_003002.4(SDHD):c.386del (p.Leu129fs)	rs864321644
NM_003002.4(SDHD):c.394del (p.Ser132fs)	rs1060503773
NM_003002.4(SDHD):c.412G>A (p.Gly138Arg)	rs786203932
NM_003002.4(SDHD):c.413G>A (p.Gly138Glu)	rs1401695686
NM_003002.4(SDHD):c.413G>T (p.Gly138Val)	rs1401695686
NM_003002.4(SDHD):c.416T>G (p.Leu139Arg)	rs80338847
NM_003002.4(SDHD):c.424_427del (p.Phe142fs)	rs2135277706
NM_003002.4(SDHD):c.443del (p.Gly148fs)	rs587776646
NM_003002.4(SDHD):c.53-1_53delinsTT	rs1566691921
NM_003002.4(SDHD):c.53-2A>C

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