"Ambry Genetics"[submitter] AND "CSK"[gene] - ClinVar - NCBI

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

Search results

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3078044	NM_004383.3(CSK):c.64G>A (p.Gly22Ser)	CSK, LOC126862181 (G22S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3078041	NM_004383.3(CSK):c.138C>G (p.Asn46Lys)	CSK, LOC126862181 (N46K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3269777	NM_004383.3(CSK):c.167G>A (p.Arg56His)	CSK, LOC126862181 (R56H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3078042	NM_004383.3(CSK):c.193G>A (p.Val65Ile)	CSK, LOC126862181 (V65I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3078043	NM_004383.3(CSK):c.281G>A (p.Arg94Gln)	CSK, LOC126862181 (R94Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558832	NM_004383.3(CSK):c.296C>T (p.Pro99Leu)	CSK, LOC126862181 (P66L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325323	NM_004383.3(CSK):c.367G>A (p.Asp123Asn)	CSK, LOC126862181 (D80N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334562	NM_004383.3(CSK):c.1034C>T (p.Thr345Met)	CSK (T312M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213883	NM_004383.3(CSK):c.1208A>G (p.Tyr403Cys)	CSK (Y360C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance