"PreventionGenetics, part of Exact Sciences"[submitter] AND "ROBO1"[ge - ClinVar

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Items: 54

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3049416	NM_002941.4(ROBO1):c.4827A>G (p.Ser1609=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder	GLikely benign
Select item 736441	NM_002941.4(ROBO1):c.4803C>T (p.Pro1601=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 2061944	NM_002941.4(ROBO1):c.4800T>G (p.Asp1600Glu)	ROBO1 (D1600E +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 713549	NM_002941.4(ROBO1):c.4744+6C>T	ROBO1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2653979	NM_002941.4(ROBO1):c.4719A>T (p.Pro1573=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 1529664	NM_002941.4(ROBO1):c.4704A>C (p.Ala1568=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GBenign
Select item 2052159	NM_002941.4(ROBO1):c.4360G>T (p.Val1454Leu)	ROBO1 (V1409L +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2715964	NM_002941.4(ROBO1):c.4302G>A (p.Ala1434=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 3060579	NM_002941.4(ROBO1):c.4283-9del	ROBO1	Deletion (intron variant)	ROBO1-related disorder	GBenign
Select item 722051	NM_002941.4(ROBO1):c.4155C>T (p.Ser1385=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 2633930	NM_002941.4(ROBO1):c.4142ACA[1] (p.Asn1382del)	ROBO1 (N1282del +2 more)	Microsatellite (inframe_indel +1 more)	ROBO1-related disorder	GUncertain significance
Select item 3031179	NM_002941.4(ROBO1):c.4131C>T (p.Ala1377=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder	GLikely benign
Select item 3050574	NM_002941.4(ROBO1):c.4002C>T (p.Ala1334=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder	GLikely benign
Select item 713785	NM_002941.4(ROBO1):c.3823T>C (p.Leu1275=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 722579	NM_002941.4(ROBO1):c.3816G>C (p.Gln1272His)	ROBO1 (Q1172H +2 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 2628772	NM_002941.4(ROBO1):c.3715C>T (p.Pro1239Ser)	ROBO1 (P1139S +2 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder	GUncertain significance
Select item 734039	NM_002941.4(ROBO1):c.3652G>A (p.Val1218Met)	ROBO1 (V1118M +2 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 3058292	NM_002941.4(ROBO1):c.3590G>C (p.Ser1197Thr)	ROBO1 (S1097T +2 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder	GUncertain significance
Select item 741220	NM_002941.4(ROBO1):c.3560C>T (p.Pro1187Leu)	ROBO1 (P1187L +2 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 560281	NM_002941.4(ROBO1):c.3503_3505dup (p.Gly1168dup)	ROBO1	Duplication (inframe_insertion)	ROBO1-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 720299	NM_002941.4(ROBO1):c.3246C>T (p.Asn1082=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
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 disorder	GUncertain significance
Select item 732586	NM_002941.4(ROBO1):c.2765G>A (p.Arg922His)	ROBO1 (R922H +1 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder +1 more	GBenign/Likely benign
Select item 725052	NM_002941.4(ROBO1):c.2615-10G>A	ROBO1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 728000	NM_002941.4(ROBO1):c.2442+7G>A	ROBO1	Single nucleotide variant (intron variant)	ROBO1-related disorder +1 more	GBenign/Likely benign
Select item 737214	NM_002941.4(ROBO1):c.2238C>T (p.Asn746=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 995979	NM_002941.4(ROBO1):c.2204G>A (p.Ser735Asn)	ROBO1 (S699N +1 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 2200009	NM_002941.4(ROBO1):c.2196C>G (p.Ala732=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 2632617	NM_002941.4(ROBO1):c.2168G>A (p.Trp723Ter)	ROBO1 (W687* +1 more)	Single nucleotide variant (nonsense)	ROBO1-related disorder	GLikely pathogenic
Select item 774169	NM_002941.4(ROBO1):c.2088+7T>G	ROBO1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2636743	NM_002941.4(ROBO1):c.1793C>G (p.Ala598Gly)	ROBO1 (A562G +1 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder	GUncertain significance
Select item 3046337	NM_002941.4(ROBO1):c.1779T>G (p.Ser593=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder	GLikely benign
Select item 1600939	NM_002941.4(ROBO1):c.1776A>G (p.Thr592=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GBenign/Likely benign
Select item 738129	NM_002941.4(ROBO1):c.1565G>A (p.Arg522Gln)	ROBO1 (R486Q +1 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 1941317	NM_002941.4(ROBO1):c.1373G>A (p.Arg458Gln)	ROBO1 (R422Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 791938	NM_002941.4(ROBO1):c.1233C>T (p.Gly411=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GBenign/Likely benign
Select item 1567266	NM_002941.4(ROBO1):c.1206C>T (p.Ser402=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GBenign
Select item 723120	NM_002941.4(ROBO1):c.1155G>A (p.Arg385=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2631840	NM_002941.4(ROBO1):c.1073G>A (p.Arg358His)	ROBO1 (R322H +1 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder	GUncertain significance
Select item 2632942	NM_002941.4(ROBO1):c.1005G>C (p.Met335Ile)	ROBO1 (M296I +1 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder	GUncertain significance
Select item 2635904	NM_002941.4(ROBO1):c.881G>A (p.Arg294Gln)	ROBO1 (R255Q +1 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder	GUncertain significance
Select item 2724535	NM_002941.4(ROBO1):c.816A>C (p.Ala272=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 3046992	NM_002941.4(ROBO1):c.779-8A>G	ROBO1	Single nucleotide variant (intron variant)	ROBO1-related disorder	GLikely benign
Select item 720246	NM_002941.4(ROBO1):c.658-7T>C	ROBO1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 3037653	NM_002941.4(ROBO1):c.455dup (p.Tyr152Ter)	ROBO1 (Y113* +1 more)	Duplication (frameshift variant +1 more)	ROBO1-related disorder	GLikely pathogenic
Select item 3049922	NM_002941.4(ROBO1):c.396A>C (p.Ile132=)	ROBO1	Single nucleotide variant (synonymous variant)	ROBO1-related disorder	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 disorder	GUncertain significance
Select item 2632397	NM_002941.4(ROBO1):c.350C>T (p.Ser117Leu)	ROBO1 (S117L +1 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder	GUncertain significance
Select item 3030270	NM_002941.4(ROBO1):c.205C>T (p.Arg69Cys)	ROBO1 (R30C +1 more)	Single nucleotide variant (missense variant)	ROBO1-related disorder	GUncertain significance
Select item 745781	NM_002941.4(ROBO1):c.178C>T (p.Arg60Cys)	ROBO1 (R21C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3057714	NM_002941.4(ROBO1):c.173-79487C>G	ROBO1	Single nucleotide variant (synonymous variant +1 more)	ROBO1-related disorder	GLikely benign
Select item 723990	NM_002941.4(ROBO1):c.159G>A (p.Ser53=)	ROBO1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 791023	NM_002941.4(ROBO1):c.88+6T>C	ROBO1	Single nucleotide variant (intron variant)	ROBO1-related disorder +1 more	GLikely benign
Select item 2633733	NM_002941.4(ROBO1):c.13C>T (p.His5Tyr)	ROBO1 (H5Y)	Single nucleotide variant (missense variant)	ROBO1-related disorder	GUncertain significance

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Items: 54