"Ambry Genetics"[submitter] AND "RPS6KB1"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2605877	NM_003161.4(RPS6KB1):c.15G>T (p.Arg5Ser)	RPS6KB1 (R5S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2336734	NM_003161.4(RPS6KB1):c.52G>A (p.Asp18Asn)	RPS6KB1 (D18N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156249	NM_003161.4(RPS6KB1):c.61G>A (p.Ala21Thr)	RPS6KB1 (A21T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2321039	NM_003161.4(RPS6KB1):c.76G>A (p.Gly26Arg)	RPS6KB1 (G26R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156247	NM_003161.4(RPS6KB1):c.115G>T (p.Gly39Cys)	RPS6KB1 (G39C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2224144	NM_003161.4(RPS6KB1):c.123G>C (p.Glu41Asp)	RPS6KB1 (E41D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156248	NM_003161.4(RPS6KB1):c.142G>T (p.Gly48Cys)	RPS6KB1 (G48C +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2220630	NM_003161.4(RPS6KB1):c.434A>G (p.Asn145Ser)	RPS6KB1 (N65S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2285461	NM_003161.4(RPS6KB1):c.1328G>A (p.Arg443Gln)	RPS6KB1 (R354Q +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2475642	NM_003161.4(RPS6KB1):c.1336G>C (p.Val446Leu)	RPS6KB1 (V366L +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2617400	NM_003161.4(RPS6KB1):c.1384T>C (p.Ser462Pro)	RPS6KB1 (S462P +6 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2474379	NM_003161.4(RPS6KB1):c.1430A>C (p.Glu477Ala)	RPS6KB1 (E424A +6 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance