Related gene-specific medical variations for Gene (Select 9475) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3351295	NM_004850.5(ROCK2):c.2T>G (p.Met1Arg)	LOC129933119, ROCK2 (M1R)	Single nucleotide variant (missense variant +2 more)	ROCK2-related disorder	GUncertain significance
Select item 3315023	NM_004850.5(ROCK2):c.53C>T (p.Pro18Leu)	LOC129933119, ROCK2 (P18L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315022	NM_004850.5(ROCK2):c.118C>T (p.Pro40Ser)	LOC129933119, ROCK2 (P40S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315021	NM_004850.5(ROCK2):c.38C>T (p.Ala13Val)	LOC129933119, ROCK2 (A13V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155694	NM_004850.5(ROCK2):c.77G>T (p.Arg26Leu)	LOC129933119, ROCK2 (R26L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155693	NM_004850.5(ROCK2):c.61G>T (p.Gly21Trp)	LOC129933119, ROCK2 (G21W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155683	NM_004850.5(ROCK2):c.17C>T (p.Pro6Leu)	LOC129933119, ROCK2 (P6L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3053510	NM_004850.5(ROCK2):c.51G>T (p.Ala17=)	LOC129933119, ROCK2	Single nucleotide variant (synonymous variant +1 more)	ROCK2-related disorder	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 disorder	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 disorder	GLikely benign
Select item 2545763	NM_004850.5(ROCK2):c.109C>T (p.Pro37Ser)	LOC129933119, ROCK2 (P37S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484460	NM_004850.5(ROCK2):c.34G>C (p.Gly12Arg)	ROCK2, LOC129933119 (G12R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360119	NM_004850.5(ROCK2):c.103C>G (p.Arg35Gly)	LOC129933119, ROCK2 (R35G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2283379	NM_004850.5(ROCK2):c.50C>T (p.Ala17Val)	LOC129933119, ROCK2 (A17V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign