ClinVar for Gene (Select 8828) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 359

<< First< Prev

Page of 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3358575	NM_003872.3(NRP2):c.165C>T (p.Cys55=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3358564	NM_003872.3(NRP2):c.1198G>A (p.Ala400Thr)	NRP2 (A400T)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3358416	NM_003872.3(NRP2):c.2692A>G (p.Thr898Ala)	NRP2 (T881A +2 more)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3358316	NM_003872.3(NRP2):c.1770G>A (p.Leu590=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3358286	NM_003872.3(NRP2):c.2425+9609G>A	NRP2	Single nucleotide variant (synonymous variant +1 more)	NRP2-related disorder	GLikely benign
Select item 3358248	NM_003872.3(NRP2):c.2343C>T (p.Ser781=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3358206	NM_003872.3(NRP2):c.2595C>T (p.Ile865=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3358169	NM_003872.3(NRP2):c.1255G>A (p.Ala419Thr)	NRP2 (A419T)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3358168	NM_003872.3(NRP2):c.2515A>G (p.Thr839Ala)	NRP2 (T822A +2 more)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
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 3358096	NM_003872.3(NRP2):c.2330G>T (p.Gly777Val)	NRP2 (G777V)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
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 3358049	NM_003872.3(NRP2):c.1406G>A (p.Ser469Asn)	NRP2 (S469N)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3357983	NM_003872.3(NRP2):c.665-8A>T	NRP2	Single nucleotide variant (intron variant)	NRP2-related disorder	GLikely benign
Select item 3357907	NM_003872.3(NRP2):c.243C>T (p.His81=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3357881	NM_003872.3(NRP2):c.929G>A (p.Arg310Gln)	NRP2 (R310Q)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3357854	NM_003872.3(NRP2):c.1254C>T (p.Ile418=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3357836	NM_003872.3(NRP2):c.1026C>T (p.Ile342=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3357821	NM_003872.3(NRP2):c.2174G>A (p.Gly725Asp)	NRP2 (G725D)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3357766	NM_003872.3(NRP2):c.2442A>G (p.Ile814Met)	NRP2 (I814M +1 more)	Single nucleotide variant (missense variant +1 more)	NRP2-related disorder	GUncertain significance
Select item 3357709	NM_003872.3(NRP2):c.2116C>A (p.Pro706Thr)	NRP2 (P706T)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3357682	NM_003872.3(NRP2):c.2425+9468G>T	NRP2 (E817D +1 more)	Single nucleotide variant (missense variant +1 more)	NRP2-related disorder	GUncertain significance
Select item 3357569	NM_003872.3(NRP2):c.2425+9654C>T	NRP2	Single nucleotide variant (synonymous variant +1 more)	NRP2-related disorder	GLikely benign
Select item 3357530	NM_003872.3(NRP2):c.2425+9557C>G	NRP2 (S847C +1 more)	Single nucleotide variant (missense variant +1 more)	NRP2-related disorder	GUncertain significance
Select item 3357472	NM_003872.3(NRP2):c.1382G>C (p.Ser461Thr)	NRP2 (S461T)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3357259	NM_003872.3(NRP2):c.94T>C (p.Leu32=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3357229	NM_003872.3(NRP2):c.2259G>C (p.Glu753Asp)	NRP2 (E753D)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3357192	NM_003872.3(NRP2):c.1903+5G>A	NRP2	Single nucleotide variant (intron variant)	NRP2-related disorder	GLikely benign
Select item 3357172	NM_003872.3(NRP2):c.2278A>G (p.Ile760Val)	NRP2 (I760V)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3357158	NM_003872.3(NRP2):c.1691A>G (p.Asp564Gly)	NRP2 (D564G)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3357026	NM_003872.3(NRP2):c.*3G>T	NRP2	Single nucleotide variant (3 prime UTR variant)	NRP2-related disorder	GLikely benign
Select item 3356964	NM_003872.3(NRP2):c.1421G>T (p.Trp474Leu)	NRP2 (W474L)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3356767	NM_003872.3(NRP2):c.2425+9434C>T	NRP2	Single nucleotide variant (intron variant)	NRP2-related disorder	GLikely benign
Select item 3356705	NM_003872.3(NRP2):c.2425+9440del	NRP2	Deletion (intron variant)	NRP2-related disorder	GLikely benign
Select item 3356299	NM_003872.3(NRP2):c.2425+9669G>A	NRP2	Single nucleotide variant (synonymous variant +1 more)	NRP2-related disorder	GLikely benign
Select item 3356201	NM_003872.3(NRP2):c.1248A>G (p.Ser416=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3355953	NM_003872.3(NRP2):c.1059G>A (p.Gln353=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3355935	NM_003872.3(NRP2):c.138C>G (p.Pro46=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3355930	NM_003872.3(NRP2):c.2142G>A (p.Val714=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3355744	NM_003872.3(NRP2):c.2425+9468G>A	NRP2	Single nucleotide variant (synonymous variant +1 more)	NRP2-related disorder	GLikely benign
Select item 3355702	NM_003872.3(NRP2):c.2279T>C (p.Ile760Thr)	NRP2 (I760T)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3355644	NM_003872.3(NRP2):c.2497A>G (p.Ser833Gly)	NRP2 (S816G +2 more)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3355485	NM_003872.3(NRP2):c.990G>C (p.Gln330His)	NRP2 (Q330H)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3355216	NM_003872.3(NRP2):c.1276G>A (p.Gly426Ser)	NRP2 (G426S)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3355204	NM_003872.3(NRP2):c.1433T>C (p.Ile478Thr)	NRP2 (I478T)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3355143	NM_003872.3(NRP2):c.2716G>A (p.Glu906Lys)	NRP2 (E889K +2 more)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3355084	NM_003872.3(NRP2):c.1631A>G (p.Gln544Arg)	NRP2 (Q544R)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3355082	NM_003872.3(NRP2):c.1903G>A (p.Asp635Asn)	NRP2 (D635N)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3354997	NM_003872.3(NRP2):c.84C>T (p.Cys28=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
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 3354796	NM_003872.3(NRP2):c.330G>A (p.Pro110=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3354735	NM_003872.3(NRP2):c.1000C>A (p.Arg334Ser)	NRP2 (R334S)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3354633	NM_003872.3(NRP2):c.2271G>A (p.Gly757=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3354597	NM_003872.3(NRP2):c.990+4C>G	NRP2	Single nucleotide variant (intron variant)	NRP2-related disorder	GLikely benign
Select item 3354550	NM_003872.3(NRP2):c.2425+9726G>A	NRP2	Single nucleotide variant (3 prime UTR variant +1 more)	NRP2-related disorder	GLikely benign
Select item 3354544	NM_003872.3(NRP2):c.527C>T (p.Thr176Ile)	NRP2 (T176I)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3354495	NM_003872.3(NRP2):c.2425+9651C>A	NRP2	Single nucleotide variant (synonymous variant +1 more)	NRP2-related disorder	GLikely benign
Select item 3354302	NM_003872.3(NRP2):c.1291+6G>A	NRP2	Single nucleotide variant (intron variant)	NRP2-related disorder	GLikely benign
Select item 3354270	NM_003872.3(NRP2):c.60G>A (p.Val20=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3354055	NM_003872.3(NRP2):c.553A>T (p.Met185Leu)	NRP2 (M185L)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3353885	NM_003872.3(NRP2):c.2327T>C (p.Ile776Thr)	NRP2 (I776T)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3353785	NM_003872.3(NRP2):c.1787-3C>T	NRP2	Single nucleotide variant (intron variant)	NRP2-related disorder	GLikely benign
Select item 3353567	NM_003872.3(NRP2):c.81G>T (p.Pro27=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3353559	NM_003872.3(NRP2):c.2045-17_2045-8del	NRP2	Deletion (intron variant)	NRP2-related disorder	GLikely benign
Select item 3353553	NM_003872.3(NRP2):c.2196G>A (p.Val732=)	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 3353458	NM_003872.3(NRP2):c.1052A>T (p.Glu351Val)	NRP2 (E351V)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3353398	NM_003872.3(NRP2):c.408T>C (p.Ser136=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3353359	NM_003872.3(NRP2):c.1283G>A (p.Arg428Gln)	NRP2 (R428Q)	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 3352512	NM_003872.3(NRP2):c.471C>T (p.Asn157=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3352499	NM_003872.3(NRP2):c.2339G>A (p.Arg780His)	NRP2 (R780H)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3352428	NM_003872.3(NRP2):c.2369G>A (p.Arg790Gln)	NRP2 (R790Q)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3352374	NM_003872.3(NRP2):c.2312T>C (p.Val771Ala)	NRP2 (V771A)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3352056	NM_003872.3(NRP2):c.1353C>T (p.Ser451=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3352036	NM_003872.3(NRP2):c.786G>A (p.Ala262=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3351927	NM_003872.3(NRP2):c.1736C>T (p.Ser579Leu)	NRP2 (S579L)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3351568	NM_003872.3(NRP2):c.2425+9532G>A	NRP2 (G839R +1 more)	Single nucleotide variant (missense variant +1 more)	NRP2-related disorder	GUncertain significance
Select item 3351520	NM_003872.3(NRP2):c.1594G>A (p.Gly532Ser)	NRP2 (G532S)	Single nucleotide variant (missense variant)	NRP2-related disorder	GLikely benign
Select item 3351467	NM_003872.3(NRP2):c.2172C>A (p.Gly724=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3351441	NM_003872.3(NRP2):c.2272C>A (p.Arg758=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3351181	NM_003872.3(NRP2):c.2595C>A (p.Ile865=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3350987	NM_003872.3(NRP2):c.2596G>A (p.Ala866Thr)	NRP2 (A849T +2 more)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3350986	NM_003872.3(NRP2):c.1879G>C (p.Gly627Arg)	NRP2 (G627R)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3350955	NM_003872.3(NRP2):c.433+8T>G	NRP2	Single nucleotide variant (intron variant)	NRP2-related disorder	GLikely benign
Select item 3350898	NM_003872.3(NRP2):c.1517C>T (p.Ala506Val)	NRP2 (A506V)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3350875	NM_003872.3(NRP2):c.1613T>C (p.Ile538Thr)	NRP2 (I538T)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3350845	NM_003872.3(NRP2):c.2425+9639C>A	NRP2	Single nucleotide variant (synonymous variant +1 more)	NRP2-related disorder	GLikely benign
Select item 3350841	NM_003872.3(NRP2):c.835G>A (p.Val279Ile)	NRP2 (V279I)	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 3350668	NM_003872.3(NRP2):c.73G>A (p.Asp25Asn)	NRP2 (D25N)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3350587	NM_003872.3(NRP2):c.664+7G>A	NRP2	Single nucleotide variant (intron variant)	NRP2-related disorder	GLikely benign
Select item 3350573	NM_003872.3(NRP2):c.1810C>G (p.Leu604Val)	NRP2 (L604V)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3350272	NM_003872.3(NRP2):c.2317G>A (p.Glu773Lys)	NRP2 (E773K)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3350267	NM_003872.3(NRP2):c.1858G>A (p.Glu620Lys)	NRP2 (E620K)	Single nucleotide variant (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3350183	NM_003872.3(NRP2):c.1673_1674delinsTG (p.Pro558Leu)	NRP2 (P558L)	Indel (missense variant)	NRP2-related disorder	GUncertain significance
Select item 3349688	NM_003872.3(NRP2):c.2425+9620A>G	NRP2 (H868R +1 more)	Single nucleotide variant (missense variant +1 more)	NRP2-related disorder	GUncertain significance
Select item 3349652	NM_003872.3(NRP2):c.1203A>G (p.Pro401=)	NRP2	Single nucleotide variant (synonymous variant)	NRP2-related disorder	GLikely benign
Select item 3349574	NM_003872.3(NRP2):c.2405-2A>G	NRP2	Single nucleotide variant (splice acceptor variant)	NRP2-related disorder	GUncertain significance

<< First< Prev

Page of 4