ClinVar for Gene (Select 101929586) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2336935	NM_014862.4(ARNT2):c.1148G>A (p.Arg383His)	ARNT2, LOC101929586 (R383H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 1949298	NM_014862.4(ARNT2):c.1125C>T (p.His375=)	ARNT2, LOC101929586	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1918767	NM_014862.4(ARNT2):c.1147C>T (p.Arg383Cys)	ARNT2, LOC101929586 (R383C)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 154952	GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3	LOC116268473, LOC116268474 +1244 more	Copy number gain	See cases	GPathogenic
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057927, LOC130057928 +1764 more	Copy number gain	See cases	GPathogenic

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