"GeneDx"[submitter] AND "RRAS"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	LOC130064925, LOC130064926 +1081 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064903, LOC130064904 +1093 more	Copy number gain	See cases	GPathogenic
Select item 928938	NM_006270.5(RRAS):c.*4A>G	RRAS	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 496319	NM_006270.5(RRAS):c.573-12G>A	RRAS	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 527794	NM_006270.5(RRAS):c.568G>C (p.Val190Leu)	RRAS (V190L)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 457989	NM_006270.5(RRAS):c.454-9T>C	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome +1 more	GLikely benign
Select item 496318	NM_006270.5(RRAS):c.454-10C>G	RRAS	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1262195	NM_006270.5(RRAS):c.454-19G>C	RRAS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316063	NM_006270.5(RRAS):c.454-44_454-43del	RRAS	Deletion (intron variant)	not provided	GLikely benign
Select item 1318026	NM_006270.5(RRAS):c.453+145A>G	RRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 496317	NM_006270.5(RRAS):c.453+20C>T	RRAS	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 457988	NM_006270.5(RRAS):c.408C>T (p.Pro136=)	RRAS	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 457987	NM_006270.5(RRAS):c.397G>A (p.Asp133Asn)	RRAS (D133N)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 457986	NM_006270.5(RRAS):c.379C>T (p.Leu127=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +2 more	GBenign/Likely benign
Select item 496315	NM_006270.5(RRAS):c.333C>T (p.Asn111=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +2 more	GBenign
Select item 1287506	NM_006270.5(RRAS):c.242-26G>A	RRAS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290261	NM_006270.5(RRAS):c.241+54G>T	RRAS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 527797	NM_006270.5(RRAS):c.174C>T (p.Tyr58=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +2 more	GBenign/Likely benign
Select item 457983	NM_006270.5(RRAS):c.154-4C>G	RRAS	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1147175	NM_006270.5(RRAS):c.154-5G>A	RRAS	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1282757	NM_006270.5(RRAS):c.154-102T>G	RRAS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277956	NM_006270.5(RRAS):c.154-169C>T	RRAS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1318005	NM_006270.5(RRAS):c.154-171dup	RRAS	Duplication (intron variant)	not provided	GLikely benign
Select item 1274983	NM_006270.5(RRAS):c.154-262G>A	RRAS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 527791	NM_006270.5(RRAS):c.145T>C (p.Phe49Leu)	RRAS (F49L)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely benign
Select item 707268	NM_006270.5(RRAS):c.54A>T (p.Gly18=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 1316397	NC_000019.10:g.49640161dup	RRAS	Duplication	not provided	GLikely benign

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Items: 27