"PreventionGenetics, part of Exact Sciences"[submitter] AND "ROR2"[gen - ClinVar

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Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 199097	NM_004560.4(ROR2):c.*16G>A	ROR2	Single nucleotide variant (3 prime UTR variant)	Brachydactyly type B1 +3 more	GBenign
Select item 2636401	NM_004560.4(ROR2):c.2729A>G (p.Gln910Arg)	ROR2 (Q910R)	Single nucleotide variant (missense variant)	ROR2-related disorder	GUncertain significance
Select item 1610228	NM_004560.4(ROR2):c.2694G>C (p.Gln898His)	ROR2 (Q898H)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2427823	NM_004560.4(ROR2):c.2645C>G (p.Ser882Cys)	ROR2 (S882C)	Single nucleotide variant (missense variant)	ROR2-related disorder +1 more	GUncertain significance
Select item 2636869	NM_004560.4(ROR2):c.2632C>G (p.Pro878Ala)	ROR2 (P878A)	Single nucleotide variant (missense variant)	ROR2-related disorder	GUncertain significance
Select item 500279	NM_004560.4(ROR2):c.2461G>A (p.Val821Ile)	ROR2 (V821I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 159818	NM_004560.4(ROR2):c.2455G>A (p.Val819Ile)	ROR2 (V819I)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign
Select item 289221	NM_004560.4(ROR2):c.2445G>A (p.Pro815=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2629088	NM_004560.4(ROR2):c.2429C>T (p.Pro810Leu)	ROR2 (P810L)	Single nucleotide variant (missense variant)	ROR2-related disorder	GUncertain significance
Select item 199096	NM_004560.4(ROR2):c.2395C>T (p.Pro799Ser)	ROR2 (P799S)	Single nucleotide variant (missense variant)	Brachydactyly type B1 +3 more	GConflicting classifications of pathogenicity
Select item 2062979	NM_004560.4(ROR2):c.2304G>A (p.Thr768=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 367498	NM_004560.4(ROR2):c.2212C>T (p.Arg738Cys)	ROR2 (R738C)	Single nucleotide variant (missense variant)	Autosomal recessive Robinow syndrome +3 more	GConflicting classifications of pathogenicity
Select item 159816	NM_004560.4(ROR2):c.2154C>T (p.Pro718=)	ROR2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 159815	NM_004560.4(ROR2):c.2088C>T (p.Tyr696=)	ROR2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 718253	NM_004560.4(ROR2):c.1863G>A (p.Val621=)	ROR2	Single nucleotide variant (synonymous variant)	Brachydactyly type B1 +3 more	GLikely benign
Select item 259430	NM_004560.4(ROR2):c.1770C>T (p.Pro590=)	ROR2	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 284609	NM_004560.4(ROR2):c.1756G>A (p.Ala586Thr)	ROR2 (A586T)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 281429	NM_004560.4(ROR2):c.1736A>T (p.Asp579Val)	ROR2 (D579V)	Single nucleotide variant (missense variant)	Brachydactyly type B1 +3 more	GConflicting classifications of pathogenicity
Select item 159811	NM_004560.4(ROR2):c.1710G>A (p.Pro570=)	ROR2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 281495	NM_004560.4(ROR2):c.1686C>T (p.His562=)	ROR2	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign
Select item 3043281	NM_004560.4(ROR2):c.1674C>T (p.His558=)	ROR2	Single nucleotide variant (synonymous variant)	ROR2-related disorder	GLikely benign
Select item 721154	NM_004560.4(ROR2):c.1524G>A (p.Thr508=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +3 more	GLikely benign
Select item 367504	NM_004560.4(ROR2):c.1491G>A (p.Pro497=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1652351	NM_004560.4(ROR2):c.1323G>A (p.Arg441=)	ROR2 (G430D)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 259429	NM_004560.4(ROR2):c.1184-39A>T	ROR2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 1088941	NM_004560.4(ROR2):c.1137G>A (p.Thr379=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 159824	NM_004560.4(ROR2):c.986G>A (p.Ser329Asn)	ROR2 (S329N)	Single nucleotide variant (missense variant)	Brachydactyly type B1 +3 more	GConflicting classifications of pathogenicity
Select item 259432	NM_004560.4(ROR2):c.938-33C>T	ROR2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 198175	NM_004560.4(ROR2):c.937+10C>T	ROR2	Single nucleotide variant (intron variant)	Brachydactyly type B1 +3 more	GBenign/Likely benign
Select item 367510	NM_004560.4(ROR2):c.935G>A (p.Arg312His)	ROR2 (R312H)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 1513231	NM_004560.4(ROR2):c.888C>T (p.Asp296=)	ROR2	Single nucleotide variant (synonymous variant)	ROR2-related disorder +3 more	GLikely benign
Select item 3053607	NM_004560.4(ROR2):c.762C>T (p.Asp254=)	ROR2	Single nucleotide variant (synonymous variant)	ROR2-related disorder	GLikely benign
Select item 367512	NM_004560.4(ROR2):c.751C>T (p.Leu251=)	ROR2	Single nucleotide variant (synonymous variant)	Autosomal recessive Robinow syndrome +3 more	GBenign/Likely benign
Select item 367513	NM_004560.4(ROR2):c.744G>A (p.Pro248=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 159821	NM_004560.4(ROR2):c.733A>G (p.Thr245Ala)	ROR2 (T245A)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 1017599	NM_004560.4(ROR2):c.725G>A (p.Arg242His)	ROR2 (R242H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 159820	NM_004560.4(ROR2):c.498T>C (p.Asp166=)	ROR2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 259431	NM_004560.4(ROR2):c.494+25G>A	ROR2	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 792334	NM_004560.4(ROR2):c.435C>T (p.Thr145=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 196393	NM_004560.4(ROR2):c.372C>T (p.Asp124=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 367518	NM_004560.4(ROR2):c.153C>T (p.Asp51=)	ROR2	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 159823	NM_004560.4(ROR2):c.98-15G>C	ROR2	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 594697	NM_004560.4(ROR2):c.37C>G (p.Leu13Val)	ROR2 (L13V)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance

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Items: 43