RASGRF2-AS1[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58096	GRCh38/hg38 5q13.3-22.1(chr5:74163186-110809453)x3	ENC1, ERAP1 +690 more	Copy number gain	See cases	GPathogenic
Select item 58788	GRCh38/hg38 5q14.1(chr5:79665668-81197686)x1	ANKRD34B, CMYA5 +40 more	Copy number loss	See cases	GUncertain significance
Select item 2593437	NM_006909.3(RASGRF2):c.13G>C (p.Val5Leu)	RASGRF2, RASGRF2-AS1 (V5L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277400	NM_006909.3(RASGRF2):c.33C>G (p.His11Gln)	RASGRF2, RASGRF2-AS1 (H11Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151834	NM_006909.3(RASGRF2):c.106G>C (p.Ala36Pro)	RASGRF2, RASGRF2-AS1 (A36P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

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