"PreventionGenetics, part of Exact Sciences"[submitter] AND "NRP1"[gen - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044311	NM_003873.7(NRP1):c.*6G>A	NRP1	Single nucleotide variant (3 prime UTR variant +1 more)	NRP1-related disorder	GLikely benign
Select item 2635875	NM_003873.7(NRP1):c.2696A>G (p.Tyr899Cys)	NRP1 (Y882C +3 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2636092	NM_003873.7(NRP1):c.2632G>A (p.Val878Met)	NRP1 (V861M +3 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3052606	NM_003873.7(NRP1):c.2631C>A (p.Val877=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign
Select item 3059358	NM_003873.7(NRP1):c.2595T>C (p.Ser865=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign
Select item 2634431	NM_003873.7(NRP1):c.2571C>G (p.Ile857Met)	NRP1 (I840M +3 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3030707	NM_003873.7(NRP1):c.2562A>G (p.Leu854=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 726098	NM_003873.7(NRP1):c.2500G>A (p.Glu834Lys)	NRP1 (E817K +3 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder +1 more	GBenign/Likely benign
Select item 3038237	NM_003873.7(NRP1):c.2490G>A (p.Thr830=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign
Select item 770962	NM_003873.7(NRP1):c.2483-3T>C	NRP1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2356266	NM_003873.7(NRP1):c.2471T>C (p.Ile824Thr)	NRP1 (I818T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3048449	NM_003873.7(NRP1):c.2431+3A>G	NRP1	Single nucleotide variant (intron variant)	NRP1-related disorder	GLikely benign
Select item 3036946	NM_003873.7(NRP1):c.2355C>T (p.Ile785=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3057448	NM_003873.7(NRP1):c.2349C>T (p.Gly783=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 770764	NM_003873.7(NRP1):c.2349C>A (p.Gly783=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3055862	NM_003873.7(NRP1):c.2343C>T (p.Phe781=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign
Select item 3036556	NM_003873.7(NRP1):c.2262G>A (p.Met754Ile)	NRP1 (M747I +2 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder +1 more	GUncertain significance
Select item 2635692	NM_003873.7(NRP1):c.2222G>A (p.Arg741His)	NRP1 (R734H +2 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3055728	NM_003873.7(NRP1):c.2197G>A (p.Val733Ile)	NRP1 (V726I +2 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GBenign
Select item 3054529	NM_003873.7(NRP1):c.2196C>A (p.His732Gln)	NRP1 (H725Q +2 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3030222	NM_003873.7(NRP1):c.2192C>T (p.Ser731Phe)	NRP1 (S724F +2 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3055156	NM_003873.7(NRP1):c.2088A>G (p.Gln696=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3051176	NM_003873.7(NRP1):c.2062+5C>T	NRP1	Single nucleotide variant (intron variant)	NRP1-related disorder	GLikely benign
Select item 3051571	NM_003873.7(NRP1):c.2040G>A (p.Thr680=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3029186	NM_003873.7(NRP1):c.1938T>C (p.Tyr646=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3032284	NM_003873.7(NRP1):c.1925-3A>C	NRP1	Single nucleotide variant (intron variant)	NRP1-related disorder	GUncertain significance
Select item 3030130	NM_003873.7(NRP1):c.1898C>T (p.Thr633Met)	NRP1 (T598M +2 more)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3036295	NM_003873.7(NRP1):c.1815C>T (p.Asp605=)	NRP1	Single nucleotide variant (synonymous variant +2 more)	NRP1-related disorder	GLikely benign
Select item 3046453	NM_003873.7(NRP1):c.1800G>A (p.Val600=)	NRP1	Single nucleotide variant (synonymous variant +2 more)	NRP1-related disorder	GLikely benign
Select item 3056401	NM_003873.7(NRP1):c.1797G>A (p.Leu599=)	NRP1	Single nucleotide variant (synonymous variant +2 more)	NRP1-related disorder	GLikely benign
Select item 3049138	NM_003873.7(NRP1):c.1788C>T (p.Asn596=)	NRP1	Single nucleotide variant (synonymous variant +2 more)	NRP1-related disorder	GLikely benign
Select item 3058542	NM_003873.7(NRP1):c.1760C>T (p.Ala587Val)	NRP1 (A587V)	Single nucleotide variant (missense variant +2 more)	NRP1-related disorder	GUncertain significance
Select item 3056018	NM_003873.7(NRP1):c.1738C>T (p.Leu580=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign
Select item 3036346	NM_003873.7(NRP1):c.1720C>G (p.Leu574Val)	NRP1 (L574V)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3048529	NM_003873.7(NRP1):c.1704A>G (p.Arg568=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3041874	NM_003873.7(NRP1):c.1683C>G (p.Phe561Leu)	NRP1 (F561L)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GBenign
Select item 2631974	NM_003873.7(NRP1):c.1676C>T (p.Thr559Met)	NRP1 (T559M)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2396241	NM_003873.7(NRP1):c.1654C>T (p.Arg552Trp)	NRP1 (R552W)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2628514	NM_003873.7(NRP1):c.1626C>T (p.Gly542=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3058668	NM_003873.7(NRP1):c.1611G>A (p.Ala537=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 2630628	NM_003873.7(NRP1):c.1609G>A (p.Ala537Thr)	NRP1 (A537T)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3061610	NM_003873.7(NRP1):c.1572G>T (p.Ser524=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3029781	NM_003873.7(NRP1):c.1572G>A (p.Ser524=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 788303	NM_003873.7(NRP1):c.1571C>T (p.Ser524Leu)	NRP1 (S524L)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3033411	NM_003873.7(NRP1):c.1566C>T (p.Asn522=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3047251	NM_003873.7(NRP1):c.1551C>T (p.Ile517=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 2635810	NM_003873.7(NRP1):c.1517G>A (p.Arg506Gln)	NRP1 (R506Q)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3033357	NM_003873.7(NRP1):c.1497C>A (p.Ile499=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 793354	NM_003873.7(NRP1):c.1467G>C (p.Leu489=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 2634146	NM_003873.7(NRP1):c.1459A>G (p.Ile487Val)	NRP1 (I487V)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3031388	NM_003873.7(NRP1):c.1425C>T (p.Pro475=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3038551	NM_003873.7(NRP1):c.1295C>T (p.Ser432Phe)	NRP1 (S432F)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3060922	NM_003873.7(NRP1):c.1266C>T (p.Tyr422=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign
Select item 3036715	NM_003873.7(NRP1):c.1263A>G (p.Val421=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 2634664	NM_003873.7(NRP1):c.1214G>A (p.Arg405Gln)	NRP1 (R405Q)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3060724	NM_003873.7(NRP1):c.1161C>T (p.Pro387=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign
Select item 3032255	NM_003873.7(NRP1):c.1109T>C (p.Ile370Thr)	NRP1 (I370T)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GLikely benign
Select item 2635826	NM_003873.7(NRP1):c.1096G>A (p.Gly366Arg)	NRP1 (G366R)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3059235	NM_003873.7(NRP1):c.1095C>T (p.Asn365=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3045961	NM_003873.7(NRP1):c.1062T>C (p.Tyr354=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3048159	NM_003873.7(NRP1):c.1029C>T (p.Gly343=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3055196	NM_003873.7(NRP1):c.1011G>A (p.Thr337=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 2636136	NM_003873.7(NRP1):c.1010C>T (p.Thr337Met)	NRP1 (T337M)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2374679	NM_003873.7(NRP1):c.1009A>G (p.Thr337Ala)	NRP1 (T337A)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2636117	NM_003873.7(NRP1):c.1000C>T (p.Arg334Cys)	NRP1 (R334C)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2634919	NM_003873.7(NRP1):c.936G>C (p.Glu312Asp)	NRP1 (E312D)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2628890	NM_003873.7(NRP1):c.920G>T (p.Arg307Leu)	NRP1 (R307L)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2628785	NM_003873.7(NRP1):c.914G>A (p.Arg305His)	NRP1 (R305H)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3036054	NM_003873.7(NRP1):c.867C>T (p.Asp289=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 782767	NM_003873.7(NRP1):c.800G>A (p.Ser267Asn)	NRP1 (S267N)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3056553	NM_003873.7(NRP1):c.747C>T (p.Thr249=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign
Select item 3032573	NM_003873.7(NRP1):c.720G>C (p.Ser240=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3030870	NM_003873.7(NRP1):c.720G>A (p.Ser240=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3040774	NM_003873.7(NRP1):c.687A>G (p.Gly229=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 2629577	NM_003873.7(NRP1):c.664C>T (p.Pro222Ser)	NRP1 (P222S)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3032725	NM_003873.7(NRP1):c.620G>A (p.Arg207His)	NRP1 (R207H)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2629207	NM_003873.7(NRP1):c.605G>C (p.Gly202Ala)	NRP1 (G202A)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2636506	NM_003873.7(NRP1):c.602C>T (p.Pro201Leu)	NRP1 (P201L)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	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 +1 more	GLikely benign
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 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 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 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 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 3048968	NM_003873.7(NRP1):c.381C>T (p.Tyr127=)	NRP1	Single nucleotide variant (synonymous variant)	NRP1-related disorder	GLikely benign
Select item 2634414	NM_003873.7(NRP1):c.365A>C (p.Lys122Thr)	NRP1 (K122T)	Single nucleotide variant (missense variant)	NRP1-related disorder	GUncertain significance
Select item 3029392	NM_003873.7(NRP1):c.271G>A (p.Asp91Asn)	NRP1 (D91N)	Single nucleotide variant (missense variant)	NRP1-related disorder	GUncertain significance
Select item 3054129	NM_003873.7(NRP1):c.258C>T (p.Tyr86=)	NRP1	Single nucleotide variant (synonymous variant)	NRP1-related disorder	GLikely benign
Select item 3033129	NM_003873.7(NRP1):c.249-6T>C	NRP1	Single nucleotide variant (intron variant)	NRP1-related disorder	GLikely benign
Select item 3046350	NM_003873.7(NRP1):c.249-9G>C	NRP1	Single nucleotide variant (intron variant)	NRP1-related disorder	GLikely benign
Select item 2634922	NM_003873.7(NRP1):c.248+3_248+6del	NRP1	Microsatellite (splice donor variant)	NRP1-related disorder	GUncertain significance
Select item 788426	NM_003873.7(NRP1):c.243C>T (p.Asp81=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 3034886	NM_003873.7(NRP1):c.227A>G (p.Asp76Gly)	NRP1 (D76G)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3030462	NM_003873.7(NRP1):c.221A>T (p.His74Leu)	NRP1 (H74L)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2208895	NM_003873.7(NRP1):c.194A>G (p.Gln65Arg)	NRP1 (Q65R)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder +1 more	GUncertain significance
Select item 2635613	NM_003873.7(NRP1):c.127G>A (p.Gly43Ser)	NRP1 (G43S)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 2631926	NM_003873.7(NRP1):c.92T>C (p.Ile31Thr)	NRP1 (I31T)	Single nucleotide variant (missense variant +1 more)	NRP1-related disorder	GUncertain significance
Select item 3036691	NM_003873.7(NRP1):c.74-4G>C	NRP1	Single nucleotide variant (intron variant)	NRP1-related disorder	GLikely benign
Select item 3033757	NM_003873.7(NRP1):c.72C>T (p.Asn24=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GLikely benign
Select item 3057002	NM_003873.7(NRP1):c.60C>T (p.Gly20=)	NRP1	Single nucleotide variant (synonymous variant +1 more)	NRP1-related disorder	GBenign

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