"PreventionGenetics, part of Exact Sciences"[submitter] AND "ROBO2"[ge - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3035762	NM_001128929.3(ROBO2):c.-3G>T	ROBO2	Single nucleotide variant (5 prime UTR variant)	ROBO2-related disorder	GLikely benign
Select item 518348	NM_001128929.3(ROBO2):c.19C>A (p.Arg7Ser)	ROBO2 (R7S)	Single nucleotide variant (missense variant)	ROBO2-related disorder +1 more	GBenign
Select item 3054800	NM_001128929.3(ROBO2):c.41C>G (p.Thr14Arg)	ROBO2 (T14R)	Single nucleotide variant (missense variant)	ROBO2-related disorder	GUncertain significance
Select item 3059790	NM_001128929.3(ROBO2):c.42A>G (p.Thr14=)	ROBO2	Single nucleotide variant (synonymous variant)	ROBO2-related disorder	GBenign
Select item 3059993	NM_001128929.3(ROBO2):c.51G>A (p.Pro17=)	ROBO2	Single nucleotide variant (synonymous variant)	ROBO2-related disorder	GBenign
Select item 3040686	NM_001128929.3(ROBO2):c.54A>G (p.Gly18=)	ROBO2	Single nucleotide variant (synonymous variant)	ROBO2-related disorder	GLikely benign
Select item 518349	NM_001128929.3(ROBO2):c.73G>A (p.Val25Met)	ROBO2 (V25M)	Single nucleotide variant (missense variant)	ROBO2-related disorder +1 more	GBenign
Select item 3060297	NM_001128929.3(ROBO2):c.75G>C (p.Val25=)	ROBO2	Single nucleotide variant (synonymous variant)	ROBO2-related disorder	GBenign
Select item 3029368	NM_001395656.1(ROBO2):c.111T>G (p.Pro37=)	ROBO2	Single nucleotide variant (synonymous variant +1 more)	ROBO2-related disorder	GLikely benign
Select item 1601252	NM_001395656.1(ROBO2):c.204G>A (p.Gly68=)	ROBO2	Single nucleotide variant (synonymous variant +1 more)	Vesicoureteral reflux 2 +2 more	GBenign/Likely benign
Select item 2369048	NM_001395656.1(ROBO2):c.251T>A (p.Leu84His)	ROBO2 (L107H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 3040898	NM_001395656.1(ROBO2):c.384G>C (p.Val128=)	ROBO2	Single nucleotide variant (synonymous variant +1 more)	ROBO2-related disorder	GLikely benign
Select item 3042679	NM_001395656.1(ROBO2):c.389-6C>A	ROBO2	Single nucleotide variant (intron variant)	ROBO2-related disorder	GLikely benign
Select item 3030436	NM_001395656.1(ROBO2):c.450A>G (p.Ala150=)	ROBO2	Single nucleotide variant (synonymous variant +1 more)	ROBO2-related disorder	GLikely benign
Select item 3044782	NM_001395656.1(ROBO2):c.618C>A (p.Thr206=)	ROBO2	Single nucleotide variant (synonymous variant +1 more)	ROBO2-related disorder	GLikely benign
Select item 2060525	NM_001395656.1(ROBO2):c.639C>G (p.Asp213Glu)	ROBO2 (D229E +2 more)	Single nucleotide variant (missense variant +1 more)	ROBO2-related disorder +1 more	GBenign/Likely benign
Select item 3043225	NM_001395656.1(ROBO2):c.668-6T>C	ROBO2	Single nucleotide variant (intron variant)	ROBO2-related disorder	GLikely benign
Select item 346683	NM_001395656.1(ROBO2):c.1072-10G>A	ROBO2	Single nucleotide variant (intron variant)	Vesicoureteral reflux 2 +2 more	GBenign
Select item 2636818	NM_001395656.1(ROBO2):c.1448G>A (p.Arg483Gln)	ROBO2 (R479Q +5 more)	Single nucleotide variant (missense variant +1 more)	ROBO2-related disorder	GUncertain significance
Select item 3041600	NM_001395656.1(ROBO2):c.1450-4C>T	ROBO2	Single nucleotide variant (intron variant)	ROBO2-related disorder	GLikely benign
Select item 2895244	NM_001395656.1(ROBO2):c.1516G>T (p.Val506Leu)	ROBO2 (V506L +5 more)	Single nucleotide variant (missense variant +1 more)	ROBO2-related disorder +1 more	GBenign
Select item 2253135	NM_001395656.1(ROBO2):c.1589C>G (p.Ser530Cys)	ROBO2 (S546C +5 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 899727	NM_001395656.1(ROBO2):c.1751A>G (p.Tyr584Cys)	ROBO2 (Y580C +5 more)	Single nucleotide variant (missense variant +1 more)	Vesicoureteral reflux 2 +2 more	GBenign
Select item 346691	NM_001395656.1(ROBO2):c.1861+8C>G	ROBO2	Single nucleotide variant (intron variant)	Vesicoureteral reflux 2 +2 more	GBenign
Select item 3050068	NM_001395656.1(ROBO2):c.1938T>C (p.His646=)	ROBO2	Single nucleotide variant (synonymous variant)	ROBO2-related disorder	GLikely benign
Select item 346696	NM_001395656.1(ROBO2):c.2030G>A (p.Arg677His)	LOC126806727, ROBO2 (R673H +6 more)	Single nucleotide variant (missense variant)	Vesicoureteral reflux 2 +2 more	GBenign/Likely benign
Select item 900886	NM_001395656.1(ROBO2):c.2058T>C (p.Ser686=)	LOC126806727, ROBO2	Single nucleotide variant (synonymous variant)	Vesicoureteral reflux 2 +1 more	GLikely benign
Select item 2721118	NM_001395656.1(ROBO2):c.2385T>G (p.Thr795=)	ROBO2	Single nucleotide variant (synonymous variant)	ROBO2-related disorder +1 more	GLikely benign
Select item 1589096	NM_001395656.1(ROBO2):c.2742T>C (p.Arg914=)	ROBO2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 718511	NM_001395656.1(ROBO2):c.2951C>T (p.Thr984Ile)	ROBO2 (T980I +6 more)	Single nucleotide variant (missense variant)	ROBO2-related disorder +1 more	GLikely benign
Select item 346705	NM_001395656.1(ROBO2):c.3420C>T (p.Gly1140=)	ROBO2	Single nucleotide variant (synonymous variant)	Vesicoureteral reflux 2 +2 more	GBenign/Likely benign
Select item 2358019	NM_001395656.1(ROBO2):c.3430T>A (p.Ser1144Thr)	ROBO2 (S1140T +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3035920	NM_001395656.1(ROBO2):c.3766G>A (p.Val1256Met)	ROBO2 (V1252M +12 more)	Single nucleotide variant (missense variant)	ROBO2-related disorder	GUncertain significance
Select item 2042195	NM_001395656.1(ROBO2):c.4264G>A (p.Gly1422Ser)	ROBO2 (G1289S +19 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2635563	NM_001395656.1(ROBO2):c.4307C>T (p.Thr1436Ile)	ROBO2 (T1303I +19 more)	Single nucleotide variant (missense variant)	ROBO2-related disorder	GUncertain significance
Select item 346714	NM_001395656.1(ROBO2):c.4341C>T (p.Gly1447=)	ROBO2	Single nucleotide variant (synonymous variant)	Vesicoureteral reflux 2 +2 more	GBenign/Likely benign

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Items: 36