"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "SD - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 258891	NM_003000.3(SDHB):c.765+13G>A	SDHB	Single nucleotide variant (intron variant)	not specified +3 more	GBenign/Likely benign
Select item 293809	NM_003000.3(SDHB):c.700C>T (p.Leu234=)	SDHB	Single nucleotide variant (synonymous variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 1425395	NM_003000.3(SDHB):c.598dup (p.Trp200fs)	SDHB (W200fs)	Duplication (frameshift variant)	Paragangliomas 4 +2 more	GPathogenic/Likely pathogenic
Select item 165179	NM_003000.3(SDHB):c.300T>C (p.Ser100=)	SDHB	Single nucleotide variant (synonymous variant)	Paragangliomas 4 +9 more	GBenign/Likely benign
Select item 258889	NM_003000.3(SDHB):c.201-36G>T	SDHB	Single nucleotide variant (intron variant)	not specified +5 more	GBenign
Select item 440258	NM_003000.3(SDHB):c.200+33G>A	SDHB	Single nucleotide variant (intron variant)	Paragangliomas 4 +1 more	GBenign
Select item 135192	NM_003000.3(SDHB):c.170A>G (p.His57Arg)	SDHB (H57R)	Single nucleotide variant (missense variant)	Pheochromocytoma +7 more	GBenign/Likely benign
Select item 39584	NM_003000.3(SDHB):c.143A>T (p.Asp48Val)	SDHB (D48V)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 239420	NM_003000.3(SDHB):c.113G>A (p.Arg38His)	SDHB (R38H)	Single nucleotide variant (missense variant)	Pheochromocytoma +8 more	GConflicting classifications of pathogenicity
Select item 44641	NM_003000.3(SDHB):c.18C>A (p.Ala6=)	SDHB	Single nucleotide variant (synonymous variant)	Gastrointestinal stromal tumor +8 more	GBenign
Select item 293817	NM_003000.3(SDHB):c.-37T>C	SDHB	Single nucleotide variant	Hereditary pheochromocytoma-paraganglioma +3 more	GBenign/Likely benign