CRK[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2257971	NM_016823.4(CRK):c.911G>A (p.Ser304Asn)	CRK (S304N)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2494755	NM_016823.4(CRK):c.895C>T (p.Pro299Ser)	CRK (P299S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2274335	NM_016823.4(CRK):c.875G>A (p.Arg292His)	CRK (R292H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3077523	NM_016823.4(CRK):c.807T>G (p.Ile269Met)	CRK (I269M)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3077521	NM_016823.4(CRK):c.681C>A (p.Asn227Lys)	CRK (N227K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269554	NM_016823.4(CRK):c.665C>A (p.Ala222Asp)	CRK (A222D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269555	NM_016823.4(CRK):c.647C>A (p.Pro216Gln)	CRK (P216Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 758881	NM_016823.4(CRK):c.600G>A (p.Leu200=)	CRK	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3077520	NM_016823.4(CRK):c.511A>C (p.Asn171His)	CRK (N171H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397529	NM_016823.4(CRK):c.376G>A (p.Gly126Arg)	CRK (G126R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775157	NM_016823.4(CRK):c.375T>C (p.Ser125=)	CRK	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2308687	NM_016823.4(CRK):c.218C>G (p.Pro73Arg)	CRK (P73R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768814	NM_016823.4(CRK):c.204C>G (p.Arg68=)	CRK	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 789896	NM_016823.4(CRK):c.180C>T (p.Tyr60=)	CRK	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3269556	NM_016823.4(CRK):c.28C>T (p.Arg10Trp)	CRK (R10W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance