"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ROR2"[gene - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 159819	NM_004560.4(ROR2):c.2805C>G (p.Asp935Glu)	ROR2 (D935E)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 1595374	NM_004560.4(ROR2):c.2604C>T (p.Ser868=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 289430	NM_004560.4(ROR2):c.2466C>T (p.Asn822=)	ROR2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 199096	NM_004560.4(ROR2):c.2395C>T (p.Pro799Ser)	ROR2 (P799S)	Single nucleotide variant (missense variant)	ROR2-related condition +3 more	GConflicting classifications of pathogenicity
Select item 500118	NM_004560.4(ROR2):c.2286G>A (p.Ser762=)	ROR2	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 159817	NM_004560.4(ROR2):c.2285C>T (p.Ser762Leu)	ROR2 (S762L)	Single nucleotide variant (missense variant)	Brachydactyly, type B1Robinow syndrome, autosomal recessive +3 more	GConflicting classifications of pathogenicity
Select item 286293	NM_004560.4(ROR2):c.2240G>A (p.Arg747Gln)	ROR2 (R747Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 159812	NM_004560.4(ROR2):c.1959G>A (p.Leu653=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 367500	NM_004560.4(ROR2):c.1820C>T (p.Ser607Phe)	ROR2 (S607F)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 289424	NM_004560.4(ROR2):c.1712A>G (p.His571Arg)	ROR2 (H571R)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 1336627	NM_004560.4(ROR2):c.1687G>A (p.Glu563Lys)	ROR2 (E563K)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 284633	NM_004560.4(ROR2):c.1589G>A (p.Arg530Gln)	ROR2 (R530Q)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 547044	NM_004560.4(ROR2):c.1322G>A (p.Arg441Gln)	ROR2 (R441Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 983455	NM_004560.4(ROR2):c.1189C>T (p.Arg397Ter)	ROR2 (R397*)	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GPathogenic
Select item 1906606	NM_004560.4(ROR2):c.1086C>T (p.His362=)	ROR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2659300	NM_004560.4(ROR2):c.1079G>C (p.Gly360Ala)	ROR2 (G360A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2659301	NM_004560.4(ROR2):c.1034C>G (p.Pro345Arg)	ROR2 (P345R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 367514	NM_004560.4(ROR2):c.717C>T (p.Cys239=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1949581	NM_004560.4(ROR2):c.378C>A (p.Asp126Glu)	ROR2 (D126E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 196393	NM_004560.4(ROR2):c.372C>T (p.Asp124=)	ROR2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 367521	NM_004560.4(ROR2):c.-91G>A	ROR2	Single nucleotide variant (5 prime UTR variant)	not provided +2 more	GBenign/Likely benign

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Items: 21