TYRO3[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 61

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330430	NM_006293.4(TYRO3):c.190T>A (p.Cys64Ser)	TYRO3 (C64S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398604	NM_006293.4(TYRO3):c.202G>C (p.Gly68Arg)	TYRO3 (G68R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251517	NM_006293.4(TYRO3):c.229G>T (p.Val77Leu)	TYRO3 (V77L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378997	NM_006293.4(TYRO3):c.284A>G (p.Glu95Gly)	TYRO3 (E95G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185262	NM_006293.4(TYRO3):c.309C>A (p.Ser103Arg)	TYRO3 (S103R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 712154	NM_006293.4(TYRO3):c.549C>T (p.Pro183=)	TYRO3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2360109	NM_006293.4(TYRO3):c.600G>A (p.Met200Ile)	TYRO3 (M155I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185263	NM_006293.4(TYRO3):c.638C>T (p.Ser213Phe)	TYRO3 (S168F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2429362	NM_006293.4(TYRO3):c.666_667insCACTGCCTGCAGCCCCCTTCAACATCACC (p.Ala223fs)	TYRO3 (A178fs +1 more)	Insertion (frameshift variant)	46,XX disorder of sex development	GUncertain significance
Select item 2225806	NM_006293.4(TYRO3):c.726T>G (p.Ser242Arg)	TYRO3 (S242R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185265	NM_006293.4(TYRO3):c.830C>T (p.Pro277Leu)	TYRO3 (P232L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354153	NM_006293.4(TYRO3):c.941C>T (p.Pro314Leu)	TYRO3 (P269L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185257	NM_006293.4(TYRO3):c.1092A>T (p.Gln364His)	TYRO3 (Q364H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330427	NM_006293.4(TYRO3):c.1178G>A (p.Arg393His)	TYRO3 (R393H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385299	NM_006293.4(TYRO3):c.1195G>A (p.Ala399Thr)	TYRO3 (A354T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344214	NM_006293.4(TYRO3):c.1246C>T (p.Arg416Cys)	TYRO3 (R416C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185258	NM_006293.4(TYRO3):c.1262G>T (p.Gly421Val)	TYRO3 (G421V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530598	NM_006293.4(TYRO3):c.1289T>C (p.Val430Ala)	TYRO3 (V385A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330429	NM_006293.4(TYRO3):c.1306G>A (p.Val436Met)	TYRO3 (V436M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185259	NM_006293.4(TYRO3):c.1330G>A (p.Ala444Thr)	TYRO3 (A399T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782786	NM_006293.4(TYRO3):c.1374G>A (p.Thr458=)	TYRO3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2526704	NM_006293.4(TYRO3):c.1469G>A (p.Arg490His)	TYRO3 (R445H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255963	NM_006293.4(TYRO3):c.1504G>A (p.Asp502Asn)	TYRO3 (D457N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235335	NM_006293.4(TYRO3):c.1505A>G (p.Asp502Gly)	TYRO3 (D457G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273342	NM_006293.4(TYRO3):c.1534C>T (p.Leu512Phe)	TYRO3 (L467F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338055	NM_006293.4(TYRO3):c.1564C>G (p.Arg522Gly)	TYRO3 (R522G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477554	NM_006293.4(TYRO3):c.1565G>A (p.Arg522Gln)	TYRO3 (R477Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 981851	NM_006293.4(TYRO3):c.1628C>T (p.Ser543Phe)	TYRO3 (S498F +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2474845	NM_006293.4(TYRO3):c.1855C>T (p.Arg619Trp)	TYRO3 (R574W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619556	NM_006293.4(TYRO3):c.1979A>T (p.Asn660Ile)	TYRO3 (N660I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769412	NM_006293.4(TYRO3):c.2005G>T (p.Val669Leu)	TYRO3 (V624L +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 784310	NM_006293.4(TYRO3):c.2023G>A (p.Gly675Arg)	TYRO3 (G675R +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3185260	NM_006293.4(TYRO3):c.2032C>T (p.Arg678Trp)	TYRO3 (R633W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602845	NM_006293.4(TYRO3):c.2059C>T (p.Arg687Cys)	TYRO3 (R687C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241311	NM_006293.4(TYRO3):c.2086G>A (p.Val696Ile)	TYRO3 (V651I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316265	NM_006293.4(TYRO3):c.2172G>C (p.Glu724Asp)	TYRO3 (E724D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364321	NM_006293.4(TYRO3):c.2182C>T (p.Arg728Cys)	TYRO3 (R683C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556902	NM_006293.4(TYRO3):c.2219A>T (p.Glu740Val)	TYRO3 (E695V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375535	NM_006293.4(TYRO3):c.2264C>T (p.Pro755Leu)	TYRO3 (P755L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290852	NM_006293.4(TYRO3):c.2268G>C (p.Glu756Asp)	TYRO3 (E711D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272924	NM_006293.4(TYRO3):c.2426G>A (p.Arg809Lys)	TYRO3 (R809K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330428	NM_006293.4(TYRO3):c.2441C>T (p.Thr814Ile)	TYRO3 (T769I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 730048	NM_006293.4(TYRO3):c.2444C>T (p.Ala815Val)	TYRO3 (A770V +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 729191	NM_006293.4(TYRO3):c.2445G>T (p.Ala815=)	TYRO3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3185261	NM_006293.4(TYRO3):c.2458G>C (p.Glu820Gln)	TYRO3 (E775Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611673	NM_006293.4(TYRO3):c.2473G>A (p.Asp825Asn)	TYRO3 (D825N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214370	NM_006293.4(TYRO3):c.2525G>A (p.Gly842Asp)	TYRO3 (G842D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474064	NM_006293.4(TYRO3):c.2629C>A (p.Leu877Ile)	TYRO3 (L832I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3243779	NC_000015.9:g.(?_38545387)_(42105565_?)dup	ANKRD63, BAHD1 +49 more	Duplication	Mosaic variegated aneuploidy syndrome 1	GUncertain significance
Select item 3063379	GRCh37/hg19 15q11.2-21.2(chr15:22770421-50347130)x3	ACTC1, ADAL +200 more	Copy number gain	not specified	GPathogenic
Select item 2671612	Single allele	ADAL, AFG2B +103 more	Deletion	not provided	GPathogenic
Select item 1024934	NC_000015.9:g.(?_32964879)_(91358519_?)dup	CGNL1, MAPDA +472 more	Duplication	Familial colorectal cancer +1 more	GUncertain significance
Select item 980031	GRCh37/hg19 15q15.1(chr15:41869275-42484890)x3	MGA, PLA2G4F +9 more	Copy number gain	not provided	GLikely benign
Select item 687641	GRCh37/hg19 15q15.1(chr15:41837513-41869276)x1	TYRO3	Copy number loss	not provided	GUncertain significance
Select item 585332	GRCh37/hg19 15q14-15.1 chr15:34638237..42057083 complex variant	CCDC32, RTF1 +60 more	Complex	Spindle cell sarcoma	GPathogenic
Select item 560049	Single allele	PDIA3, PEAK1 +521 more	Duplication	not provided	GPathogenic
Select item 442893	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3	AAGAB, ABHD17C +559 more	Copy number gain	See cases	GPathogenic
Select item 442892	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)	NOX5, NPAP1 +559 more	Copy number gain	See cases	GPathogenic
Select item 395389	GRCh37/hg19 15q15.1-21.2(chr15:41689327-52446981)x1	ADAL, AFG2B +107 more	Copy number loss	See cases	GPathogenic
Select item 395145	GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4	CHRFAM7A, CHRM5 +566 more	Copy number gain	See cases	GPathogenic
Select item 394887	GRCh37/hg19 15q15.1-26.3(chr15:41745084-102354798)x4	ALDH1A2, ALDH1A3 +444 more	Copy number gain	See cases	GPathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 61