Related gene-specific medical variations for Gene (Select 8828) - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3358100	NM_003872.3(NRP2):c.1935T>C (p.Asn645=)	LOC126806481, NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3358092	NM_003872.3(NRP2):c.1913T>C (p.Leu638Ser)	LOC126806481, NRP2 (L638S)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3358083	NM_003872.3(NRP2):c.1954G>A (p.Glu652Lys)	LOC126806481, NRP2 (E652K)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3354876	NM_003872.3(NRP2):c.1926G>A (p.Ser642=)	LOC126806481, NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3353484	NM_003872.3(NRP2):c.2029G>A (p.Asp677Asn)	LOC126806481, NRP2 (D677N)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3353262	NM_003872.3(NRP2):c.1905C>A (p.Asp635Glu)	LOC126806481, NRP2 (D635E)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3350753	NM_003872.3(NRP2):c.2036C>T (p.Thr679Met)	LOC126806481, NRP2 (T679M)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3348618	NM_003872.3(NRP2):c.1920C>T (p.Leu640=)	LOC126806481, NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3301078	NM_003872.3(NRP2):c.1997G>A (p.Arg666Gln)	NRP2, LOC126806481 (R666Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301077	NM_003872.3(NRP2):c.1925C>T (p.Ser642Leu)	LOC126806481, NRP2 (S642L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3050557	NM_003872.3(NRP2):c.2033G>A (p.Arg678Gln)	LOC126806481, NRP2 (R678Q)	Single nucleotide variant (missense variant)	NRP2-related disorder	GLikely benign
Select item 3050242	NM_003872.3(NRP2):c.1989G>A (p.Lys663=)	LOC126806481, NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3030627	NM_003872.3(NRP2):c.2028C>T (p.Asn676=)	LOC126806481, NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3030304	NM_003872.3(NRP2):c.2037G>A (p.Thr679=)	LOC126806481, NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3029432	NM_003872.3(NRP2):c.1944C>T (p.Phe648=)	LOC126806481, NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 2636058	NM_003872.3(NRP2):c.2029G>T (p.Asp677Tyr)	LOC126806481, NRP2 (D677Y)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 2635803	NM_003872.3(NRP2):c.1996C>T (p.Arg666Trp)	LOC126806481, NRP2 (R666W)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 2477533	NM_003872.3(NRP2):c.2026A>C (p.Asn676His)	LOC126806481, NRP2 (N676H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 741818	NM_003872.3(NRP2):c.1953C>T (p.Leu651=)	LOC126806481, NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign