ClinVar for Gene (Select 129998839) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2405675	NM_020186.3(SDHAF3):c.73C>T (p.Pro25Ser)	LOC129998839, SDHAF3 (P25S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 153321	GRCh38/hg38 7q21.2-21.3(chr7:92759144-97568646)x1	LOC110121296, LOC111365161 +110 more	Copy number loss	See cases	GPathogenic
Select item 152344	GRCh38/hg38 7q21.3(chr7:96924153-97157268)x1	DLX5, DLX6 +9 more	Copy number loss	See cases	GPathogenic
Select item 146112	GRCh38/hg38 7q21.3(chr7:95127070-97873487)x1	ASB4, ASNS +61 more	Copy number loss	See cases	GPathogenic
Select item 146075	GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	CUL1, CUX1 +4737 more	Copy number loss	See cases	GPathogenic

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