"GeneDx"[submitter] AND "RRAS2"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1288635	NM_012250.6(RRAS2):c.*124G>C	RRAS2	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 3373746	NM_012250.6(RRAS2):c.489T>A (p.Asn163Lys)	RRAS2 (N128K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368491	NM_012250.6(RRAS2):c.451G>A (p.Val151Ile)	RRAS2 (V116I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1270813	NM_012250.6(RRAS2):c.409-16A>T	RRAS2	Single nucleotide variant (intron variant)	RASopathy	GBenign FDA Recognized database
Select item 1238516	NM_012250.6(RRAS2):c.408+102G>A	RRAS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281308	NM_012250.6(RRAS2):c.408+89dup	RRAS2	Duplication (intron variant)	not provided	GBenign
Select item 1237157	NM_012250.6(RRAS2):c.300-4del	RRAS2	Deletion (intron variant)	not provided	GBenign
Select item 1198070	NM_012250.6(RRAS2):c.247A>T (p.Met83Leu)	RRAS2 (M48L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2136007	NM_012250.6(RRAS2):c.108+509A>G	RRAS2	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1254623	NM_012250.6(RRAS2):c.98A>G (p.Gln33Arg)	RRAS2 (Q33R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1201613	NM_012250.6(RRAS2):c.62_73dup (p.Gly21_Gly24dup)	LOC130005368, RRAS2	Duplication (inframe_insertion +1 more)	not provided	GLikely pathogenic
Select item 2446526	NM_012250.6(RRAS2):c.71G>A (p.Gly24Asp)	LOC130005368, RRAS2 (G24D)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic
Select item 1699117	NM_012250.6(RRAS2):c.68G>A (p.Gly23Asp)	LOC130005368, RRAS2 (G23D)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic
Select item 626911	NM_012250.6(RRAS2):c.68G>T (p.Gly23Val)	LOC130005368, RRAS2 (G23V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic
Select item 1342092	NM_012250.6(RRAS2):c.67G>T (p.Gly23Cys)	LOC130005368, RRAS2 (G23C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1252817	NM_001177314.2(RRAS2):c.3+5109C>T	LOC130005368, RRAS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262103	NM_001177314.2(RRAS2):c.-2C>T	RRAS2	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1255290	NC_000011.10:g.14364599A>G	RRAS2	Single nucleotide variant	not provided	GBenign