"ROCK2-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039060	NM_004850.5(ROCK2):c.3606A>C (p.Ile1202=)	ROCK2	Single nucleotide variant (synonymous variant)	ROCK2-related condition	GBenign
Select item 2633977	NM_004850.5(ROCK2):c.2830A>T (p.Ile944Phe)	ROCK2 (I858F +1 more)	Single nucleotide variant (missense variant)	ROCK2-related condition	GUncertain significance
Select item 3033917	NM_004850.5(ROCK2):c.2620-6A>G	ROCK2	Single nucleotide variant (intron variant)	ROCK2-related condition	GBenign
Select item 2632574	NM_004850.5(ROCK2):c.2588A>C (p.Gln863Pro)	ROCK2 (Q777P +1 more)	Single nucleotide variant (missense variant)	ROCK2-related condition	GUncertain significance
Select item 3061202	NM_004850.5(ROCK2):c.2583G>A (p.Glu861=)	ROCK2	Single nucleotide variant (synonymous variant)	ROCK2-related condition	GLikely benign
Select item 3030605	NM_004850.5(ROCK2):c.2550-8C>G	ROCK2	Single nucleotide variant (intron variant)	ROCK2-related condition	GLikely benign
Select item 3052771	NM_004850.5(ROCK2):c.2460A>C (p.Leu820=)	ROCK2	Single nucleotide variant (synonymous variant)	ROCK2-related condition	GBenign
Select item 3029203	NM_004850.5(ROCK2):c.2378C>T (p.Thr793Ile)	ROCK2 (T707I +1 more)	Single nucleotide variant (missense variant)	ROCK2-related condition	GUncertain significance
Select item 3050996	NM_004850.5(ROCK2):c.2172C>T (p.Ser724=)	ROCK2	Single nucleotide variant (synonymous variant)	ROCK2-related condition	GLikely benign
Select item 3046297	NM_004850.5(ROCK2):c.1689+9A>C	ROCK2	Single nucleotide variant (intron variant)	ROCK2-related condition	GLikely benign
Select item 3047934	NM_004850.5(ROCK2):c.1332+8G>T	ROCK2	Single nucleotide variant (intron variant)	ROCK2-related condition	GLikely benign
Select item 3039798	NM_004850.5(ROCK2):c.435C>T (p.Ala145=)	ROCK2	Single nucleotide variant (synonymous variant)	ROCK2-related condition	GBenign
Select item 755774	NM_004850.5(ROCK2):c.407T>G (p.Phe136Cys)	ROCK2 (F50C +1 more)	Single nucleotide variant (missense variant)	ROCK2-related condition +1 more	GLikely benign
Select item 3049867	NM_004850.5(ROCK2):c.121A>G (p.Ile41Val)	LOC129933119, ROCK2 (I41V)	Single nucleotide variant (missense variant +1 more)	ROCK2-related condition	GLikely benign
Select item 3053510	NM_004850.5(ROCK2):c.51G>T (p.Ala17=)	LOC129933119, ROCK2	Single nucleotide variant (synonymous variant +1 more)	ROCK2-related condition	GLikely benign
Select item 3033972	NM_004850.5(ROCK2):c.12C>T (p.Pro4=)	LOC129933119, ROCK2	Single nucleotide variant (synonymous variant +1 more)	ROCK2-related condition	GLikely benign