ClinVar for Gene (Select 6091) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3155596	NM_002941.4(ROBO1):c.653T>G (p.Ile218Arg)	ROBO1 (I179R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155595	NM_002941.4(ROBO1):c.4935A>T (p.Glu1645Asp)	ROBO1 (E1600D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155594	NM_002941.4(ROBO1):c.4819A>G (p.Met1607Val)	ROBO1 (M1507V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155593	NM_002941.4(ROBO1):c.4652G>T (p.Arg1551Ile)	ROBO1 (R1451I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155592	NM_002941.4(ROBO1):c.4652G>A (p.Arg1551Lys)	ROBO1 (R1451K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155591	NM_002941.4(ROBO1):c.4415G>A (p.Arg1472His)	ROBO1 (R1372H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155590	NM_002941.4(ROBO1):c.4232C>T (p.Ala1411Val)	ROBO1 (A1411V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155589	NM_002941.4(ROBO1):c.4006A>G (p.Met1336Val)	ROBO1 (M1336V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155588	NM_002941.4(ROBO1):c.3907C>T (p.Arg1303Trp)	ROBO1 (R1303W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155587	NM_002941.4(ROBO1):c.3543C>G (p.Asn1181Lys)	ROBO1 (N1081K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155586	NM_002941.4(ROBO1):c.3520G>T (p.Val1174Leu)	ROBO1 (V1074L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155585	NM_002941.4(ROBO1):c.3227C>G (p.Thr1076Ser)	ROBO1 (T1031S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155584	NM_002941.4(ROBO1):c.3032G>A (p.Arg1011His)	ROBO1 (R1011H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155583	NM_002941.4(ROBO1):c.2021G>C (p.Gly674Ala)	ROBO1 (G674A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3060579	NM_002941.4(ROBO1):c.4283-9del	ROBO1	Deletion (intron variant)	ROBO1-related condition	GBenign
Select item 3058292	NM_002941.4(ROBO1):c.3590G>C (p.Ser1197Thr)	ROBO1 (S1097T +2 more)	Single nucleotide variant (missense variant)	ROBO1-related condition	GUncertain significance
Select item 3057714	NM_002941.4(ROBO1):c.173-79487C>G	ROBO1	Single nucleotide variant (synonymous variant +1 more)	ROBO1-related condition	GLikely benign
Select item 3050669	NM_002941.4(ROBO1):c.394A>G (p.Ile132Val)	ROBO1 (I132V +1 more)	Single nucleotide variant (missense variant)	ROBO1-related condition	GUncertain significance
Select item 3050574	NM_002941.4(ROBO1):c.4002C>T (p.Ala1334=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related condition	GLikely benign
Select item 3049922	NM_002941.4(ROBO1):c.396A>C (p.Ile132=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related condition	GLikely benign
Select item 3049416	NM_002941.4(ROBO1):c.4827A>G (p.Ser1609=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related condition	GLikely benign
Select item 3046992	NM_002941.4(ROBO1):c.779-8A>G	ROBO1	Single nucleotide variant (intron variant)	ROBO1-related condition	GLikely benign
Select item 3046337	NM_002941.4(ROBO1):c.1779T>G (p.Ser593=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related condition	GLikely benign
Select item 3037653	NM_002941.4(ROBO1):c.455dup (p.Tyr152Ter)	ROBO1 (Y113* +1 more)	Duplication (frameshift variant +1 more)	ROBO1-related condition	GLikely pathogenic
Select item 3034574	NM_002941.4(ROBO1):c.3166C>A (p.Pro1056Thr)	ROBO1 (P1011T +1 more)	Single nucleotide variant (missense variant +1 more)	ROBO1-related condition	GUncertain significance
Select item 3031179	NM_002941.4(ROBO1):c.4131C>T (p.Ala1377=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related condition	GLikely benign
Select item 3030270	NM_002941.4(ROBO1):c.205C>T (p.Arg69Cys)	ROBO1 (R30C +1 more)	Single nucleotide variant (missense variant)	ROBO1-related condition	GUncertain significance
Select item 3012436	NM_002941.4(ROBO1):c.2882+13_2882+16del	ROBO1	Microsatellite (intron variant)	not provided	GLikely benign
Select item 3011036	NM_002941.4(ROBO1):c.296T>C (p.Ile99Thr)	ROBO1 (I60T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3009721	NM_002941.4(ROBO1):c.2298G>A (p.Lys766=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3009110	NM_002941.4(ROBO1):c.769_772del (p.Thr257fs)	ROBO1 (T218fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3009105	NM_002941.4(ROBO1):c.1630+10A>G	ROBO1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3007606	NM_002941.4(ROBO1):c.4435+16C>T	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3006852	NM_002941.4(ROBO1):c.2592T>C (p.Ser864=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3003969	NM_002941.4(ROBO1):c.3627-17C>T	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3003131	NM_002941.4(ROBO1):c.3821T>C (p.Met1274Thr)	ROBO1 (M1174T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3003053	NM_002941.4(ROBO1):c.4677C>T (p.Asp1559=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3000829	NM_002941.4(ROBO1):c.4283-11T>C	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3000387	NM_002941.4(ROBO1):c.85C>T (p.Pro29Ser)	ROBO1 (P29S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2996964	NM_002941.4(ROBO1):c.3875+13T>C	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2994903	NM_002941.4(ROBO1):c.2201A>G (p.Asn734Ser)	ROBO1 (N698S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2994894	NM_002941.4(ROBO1):c.630A>G (p.Pro210=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2993439	NM_002941.4(ROBO1):c.1045+3A>G	ROBO1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2988372	NM_002941.4(ROBO1):c.1363C>A (p.Pro455Thr)	ROBO1 (P419T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2988262	NM_002941.4(ROBO1):c.2614+18T>C	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986936	NM_002941.4(ROBO1):c.2089-12T>C	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986349	NM_002941.4(ROBO1):c.2839+13_2839+18del	ROBO1	Deletion (intron variant)	not provided	GLikely benign
Select item 2985377	NM_002941.4(ROBO1):c.2615-17G>A	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2984950	NM_002941.4(ROBO1):c.2883-17A>T	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2969669	NM_002941.4(ROBO1):c.311G>T (p.Gly104Val)	ROBO1 (G65V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2964233	NM_002941.4(ROBO1):c.4873A>G (p.Arg1625Gly)	ROBO1 (R1525G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2963815	NM_002941.4(ROBO1):c.3849C>T (p.Gly1283=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2958682	NM_002941.4(ROBO1):c.1102G>A (p.Val368Ile)	ROBO1 (V368I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2958665	NM_002941.4(ROBO1):c.2840-14dup	ROBO1	Duplication (intron variant)	not provided	GBenign
Select item 2917241	NM_002941.4(ROBO1):c.1355G>A (p.Arg452Gln)	ROBO1 (R416Q +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2909534	NM_002941.4(ROBO1):c.2883G>A (p.Arg961=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2907642	NM_002941.4(ROBO1):c.2190G>A (p.Thr730=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2901587	NM_002941.4(ROBO1):c.907C>T (p.Pro303Ser)	ROBO1 (P264S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2896857	NM_002941.4(ROBO1):c.2460T>C (p.Asn820=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2896856	NM_002941.4(ROBO1):c.4329C>T (p.Pro1443=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2895392	NM_002941.4(ROBO1):c.16G>A (p.Val6Ile)	ROBO1 (V6I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2892064	NM_002941.4(ROBO1):c.4357G>A (p.Ala1453Thr)	ROBO1 (A1408T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2891298	NM_002941.4(ROBO1):c.4364T>C (p.Met1455Thr)	ROBO1 (M1355T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2890989	NM_002941.4(ROBO1):c.3854T>G (p.Met1285Arg)	ROBO1 (M1240R +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2885607	NM_002941.4(ROBO1):c.1944A>G (p.Ile648Met)	ROBO1 (I612M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2885174	NM_002941.4(ROBO1):c.4050G>T (p.Gly1350=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2883310	NM_002941.4(ROBO1):c.1628A>C (p.Gln543Pro)	ROBO1 (Q507P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2883305	NM_002941.4(ROBO1):c.2203A>T (p.Ser735Cys)	ROBO1 (S699C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2882466	NM_002941.4(ROBO1):c.1025C>A (p.Ser342Tyr)	ROBO1 (S303Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2880251	NM_002941.4(ROBO1):c.3782C>T (p.Ala1261Val)	ROBO1 (A1216V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2880187	NM_002941.4(ROBO1):c.4744+17del	ROBO1	Deletion (intron variant)	not provided	GLikely benign
Select item 2877039	NM_002941.4(ROBO1):c.3643C>T (p.Pro1215Ser)	ROBO1 (P1170S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2877025	NM_002941.4(ROBO1):c.3952del (p.Leu1318fs)	ROBO1 (L1318fs +2 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2874008	NM_002941.4(ROBO1):c.4540A>G (p.Met1514Val)	ROBO1 (M1414V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2869787	NM_002941.4(ROBO1):c.2883-12T>C	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2852817	NM_002941.4(ROBO1):c.731A>G (p.Asn244Ser)	ROBO1 (N244S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2844580	NM_002941.4(ROBO1):c.4080G>T (p.Gly1360=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2842910	NM_002941.4(ROBO1):c.2324C>T (p.Pro775Leu)	ROBO1 (P739L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2826192	NM_002941.4(ROBO1):c.1116T>A (p.Cys372Ter)	ROBO1 (C372* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2817126	NM_002941.4(ROBO1):c.4049G>C (p.Gly1350Ala)	ROBO1 (G1350A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2808190	NM_002941.4(ROBO1):c.4950A>T (p.Glu1650Asp)	ROBO1 (E1650D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2796696	NM_002941.4(ROBO1):c.1942A>G (p.Ile648Val)	ROBO1 (I648V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2796275	NM_002941.4(ROBO1):c.2883-17del	ROBO1	Deletion (intron variant)	not provided	GLikely benign
Select item 2793979	NM_002941.4(ROBO1):c.2237A>G (p.Asn746Ser)	ROBO1 (N710S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2787566	NM_002941.4(ROBO1):c.4654G>A (p.Glu1552Lys)	ROBO1 (E1507K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2785814	NM_002941.4(ROBO1):c.2829C>A (p.Phe943Leu)	ROBO1 (F943L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2785119	NM_002941.4(ROBO1):c.2839+10del	ROBO1	Deletion (intron variant)	not provided	GLikely benign
Select item 2778875	NM_002941.4(ROBO1):c.4462C>G (p.Pro1488Ala)	ROBO1 (P1443A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2778428	NM_002941.4(ROBO1):c.4484C>G (p.Ala1495Gly)	ROBO1 (A1395G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2767018	NM_002941.4(ROBO1):c.4744+4C>G	ROBO1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2757893	NM_002941.4(ROBO1):c.3463C>G (p.Arg1155Gly)	ROBO1 (R1110G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2753920	NM_002941.4(ROBO1):c.2172A>G (p.Leu724=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2753033	NM_002941.4(ROBO1):c.1906G>A (p.Ala636Thr)	ROBO1 (A600T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2751666	NM_002941.4(ROBO1):c.2089-13G>C	ROBO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2749619	NM_002941.4(ROBO1):c.4414C>T (p.Arg1472Cys)	ROBO1 (R1372C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2741104	NM_002941.4(ROBO1):c.372T>C (p.Ser124=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2724535	NM_002941.4(ROBO1):c.816A>C (p.Ala272=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related condition +1 more	GLikely benign
Select item 2723646	NM_002941.4(ROBO1):c.4606G>A (p.Asp1536Asn)	ROBO1 (D1491N +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2715964	NM_002941.4(ROBO1):c.4302G>A (p.Ala1434=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related condition +1 more	GLikely benign
Select item 2711999	NM_002941.4(ROBO1):c.1356G>A (p.Arg452=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided	GBenign

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