Related gene-specific medical variations for Gene (Select 8829) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3357354	NM_003873.7(NRP1):c.525T>C (p.Tyr175=)	LOC126860910, NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3356801	NM_003873.7(NRP1):c.431-5C>A	LOC126860910, NRP1	Single nucleotide variant (intron variant)	NRP1-related disorder	GLikely benign
Select item 3356509	NM_003873.7(NRP1):c.526A>G (p.Ile176Val)	LOC126860910, NRP1 (I176V)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3355983	NM_003873.7(NRP1):c.516A>G (p.Glu172=)	LOC126860910, NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3354097	NM_003873.7(NRP1):c.507C>T (p.Asn169=)	LOC126860910, NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3354002	NM_003873.7(NRP1):c.431-3T>C	LOC126860910, NRP1	Single nucleotide variant (intron variant)	NRP1-related disorder	GLikely benign
Select item 3352128	NM_003873.7(NRP1):c.431-5C>T	LOC126860910, NRP1	Single nucleotide variant (intron variant)	NRP1-related disorder	GLikely benign
Select item 3350606	NM_003873.7(NRP1):c.511C>T (p.Leu171Phe)	LOC126860910, NRP1 (L171F)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3348053	NM_003873.7(NRP1):c.469G>A (p.Val157Met)	LOC126860910, NRP1 (V157M)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3202192	NM_003873.7(NRP1):c.484G>A (p.Gly162Arg)	LOC126860910, NRP1 (G162R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3059652	NM_003873.7(NRP1):c.537G>A (p.Val179=)	LOC126860910, NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign
Select item 3054218	NM_003873.7(NRP1):c.456A>G (p.Thr152=)	LOC126860910, NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3041270	NM_003873.7(NRP1):c.531C>A (p.Val177=)	LOC126860910, NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 2629378	NM_003873.7(NRP1):c.465T>A (p.Ser155Arg)	LOC126860910, NRP1 (S155R)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2628920	NM_003873.7(NRP1):c.466G>A (p.Gly156Arg)	LOC126860910, NRP1 (G156R)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2324670	NM_003873.7(NRP1):c.475A>G (p.Lys159Glu)	LOC126860910, NRP1 (K159E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 780136	NM_003873.7(NRP1):c.549A>G (p.Ser183=)	LOC126860910, NRP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign