"KRAS-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 45129	NM_004985.5(KRAS):c.528GAA[1] (p.Lys180del)	KRAS (K180del)	Microsatellite (3 prime UTR variant +1 more)	RASopathy	GBenign FDA Recognized database
Select item 12595	NM_033360.4(KRAS):c.*22C>G	KRAS (F156L)	Single nucleotide variant (3 prime UTR variant +1 more)	RASopathy +2 more	GPathogenic
Select item 46542	NM_004985.5(KRAS):c.451-5535A>C	KRAS (M189L)	Single nucleotide variant (missense variant +1 more)	KRAS-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 632869	NM_004985.5(KRAS):c.451-5538A>G	KRAS (I188V)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 46540	NM_004985.5(KRAS):c.451-5565G>A	KRAS (G179S)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 386200	NM_004985.5(KRAS):c.451-5604T>C	KRAS (Y166H)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1218871	NM_004985.5(KRAS):c.411T>C (p.Tyr137=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy +2 more	GLikely benign
Select item 167235	NM_004985.5(KRAS):c.291-10del	KRAS	Deletion (intron variant)	KRAS-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 227471	NM_004985.5(KRAS):c.264A>G (p.Lys88=)	KRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +4 more	GConflicting classifications of pathogenicity
Select item 40456	NM_033360.4(KRAS):c.249C>T (p.Ala83=)	KRAS	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 163768	NM_004985.5(KRAS):c.108A>G (p.Ile36Met)	KRAS (I36M)	Single nucleotide variant (missense variant)	KRAS-related disorder +6 more	GPathogenic/Likely pathogenic
Select item 2630513	NM_004985.5(KRAS):c.101C>A (p.Pro34Gln)	KRAS (P34Q)	Single nucleotide variant (missense variant)	KRAS-related disorder	GLikely pathogenic
Select item 195234	NM_033360.4(KRAS):c.93A>G (p.Glu31=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy +3 more	GConflicting classifications of pathogenicity
Select item 12580	NM_004985.5(KRAS):c.38G>A (p.Gly13Asp)	KRAS (G13D)	Single nucleotide variant (missense variant)	RASopathy +6 more	GConflicting classifications of pathogenicity
Select item 45122	NM_004985.5(KRAS):c.35G>C (p.Gly12Ala)	KRAS (G12A)	Single nucleotide variant (missense variant)	KRAS-related disorder	GLikely pathogenic
Select item 12596	NM_004985.5(KRAS):c.13A>G (p.Lys5Glu)	KRAS (K5E)	Single nucleotide variant (missense variant)	RASopathy +4 more	GPathogenic/Likely pathogenic
Select item 3046122	NM_004985.5(KRAS):c.-169_-149del	KRAS, LOC130007561	Deletion (5 prime UTR variant)	KRAS-related disorder	GLikely benign
Select item 163771	NM_004985.5(KRAS):c.-160A>G	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	RASopathy	GBenign FDA Recognized database
Select item 3061523	NM_004985.5(KRAS):c.-167A>C	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	KRAS-related disorder	GLikely benign