"RRAS-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2506325	NM_006270.5(RRAS):c.*5G>A	RRAS	Single nucleotide variant (3 prime UTR variant)	RRAS-related condition +1 more	GConflicting classifications of pathogenicity
Select item 928938	NM_006270.5(RRAS):c.*4A>G	RRAS	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 1665914	NM_006270.5(RRAS):c.645C>T (p.Cys215=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +2 more	GLikely benign
Select item 1752782	NM_006270.5(RRAS):c.630C>T (p.Gly210=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
Select item 2725369	NM_006270.5(RRAS):c.609C>T (p.Pro203=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GLikely benign
Select item 457990	NM_006270.5(RRAS):c.600G>A (p.Pro200=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +2 more	GBenign/Likely benign
Select item 928936	NM_006270.5(RRAS):c.563G>A (p.Arg188Gln)	RRAS (R188Q)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1554536	NM_006270.5(RRAS):c.516G>A (p.Ser172=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition +2 more	GLikely benign
Select item 759077	NM_006270.5(RRAS):c.454-9T>A	RRAS	Single nucleotide variant (intron variant)	RRAS-related condition +1 more	GLikely benign
Select item 1512263	NM_006270.5(RRAS):c.453+5G>A	RRAS	Single nucleotide variant (intron variant)	RRAS-related condition +1 more	GConflicting classifications of pathogenicity
Select item 457987	NM_006270.5(RRAS):c.397G>A (p.Asp133Asn)	RRAS (D133N)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 707745	NM_006270.5(RRAS):c.396C>T (p.Arg132=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
Select item 457986	NM_006270.5(RRAS):c.379C>T (p.Leu127=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +3 more	GBenign/Likely benign
Select item 706868	NM_006270.5(RRAS):c.255G>A (p.Ala85=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 527791	NM_006270.5(RRAS):c.145T>C (p.Phe49Leu)	RRAS (F49L)	Single nucleotide variant (missense variant)	not provided +3 more	GLikely benign
Select item 842327	NM_006270.5(RRAS):c.94C>T (p.Leu32=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +2 more	GLikely benign
Select item 1503389	NM_006270.5(RRAS):c.81C>T (p.Ser27=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition +2 more	GConflicting classifications of pathogenicity
Select item 3039282	NM_006270.5(RRAS):c.60G>C (p.Gly20=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition	GLikely benign
Select item 3039264	NM_006270.5(RRAS):c.57T>C (p.Pro19=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition	GLikely benign
Select item 3039001	NM_006270.5(RRAS):c.54A>C (p.Gly18=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition	GLikely benign
Select item 1646121	NM_006270.5(RRAS):c.43C>A (p.Arg15=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
Select item 3039622	NM_006270.5(RRAS):c.39G>T (p.Arg13=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition	GLikely benign
Select item 2631818	NM_006270.5(RRAS):c.9C>G (p.Ser3Arg)	RRAS (S3R)	Single nucleotide variant (missense variant)	RRAS-related condition	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 23