Related gene-specific medical variations for Gene (Select 26750) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3247985	NC_000001.10:g.(?_213224747)_(213224871_?)dup	RPS6KC1	Duplication	not provided	GUncertain significance
Select item 2972006	NM_012424.6(RPS6KC1):c.55G>A (p.Glu19Lys)	LOC129932493, RPS6KC1 (E19K)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2265450	NM_012424.6(RPS6KC1):c.58C>A (p.Pro20Thr)	LOC129932493, RPS6KC1 (P20T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1941338	NM_012424.6(RPS6KC1):c.20G>T (p.Arg7Leu)	LOC129932493, RPS6KC1 (R7L)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 1578508	NM_012424.6(RPS6KC1):c.33G>A (p.Leu11=)	LOC129932493, RPS6KC1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1547956	NM_012424.6(RPS6KC1):c.42C>T (p.Phe14=)	LOC129932493, RPS6KC1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 161662	NM_012424.6(RPS6KC1):c.3163T>C (p.Phe1055Leu)	RPS6KC1 (F1055L +9 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance

ClinVar