HAUS3[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2579172	GRCh38/hg38 4p16.3-11(chr4:1-49062177)x3	LOC123477714, LOC123477715 +1267 more	Copy number gain	Neurodevelopmental disorder	GPathogenic
Select item 155180	GRCh38/hg38 4p16.3(chr4:36424-3881330)x1	ADD1, ADRA2C +279 more	Copy number loss	See cases	GPathogenic
Select item 154884	GRCh38/hg38 4p16.3-16.1(chr4:36424-7359817)x1	ADD1, ADRA2C +426 more	Copy number loss	See cases	GPathogenic
Select item 150615	GRCh38/hg38 4p16.3(chr4:36424-3974044)x1	ADD1, ADRA2C +283 more	Copy number loss	See cases	GPathogenic
Select item 150606	GRCh38/hg38 4p16.3(chr4:36424-4097002)x3	LOC129991977, LOC129991978 +283 more	Copy number gain	See cases	GPathogenic
Select item 150122	GRCh38/hg38 4p16.3(chr4:36424-3265531)x1	ADD1, ATP5ME +250 more	Copy number loss	See cases	GPathogenic
Select item 149173	GRCh38/hg38 4p16.3-16.1(chr4:36424-9369341)x1	NELFA, NICOL1 +504 more	Copy number loss	See cases	GPathogenic
Select item 148186	GRCh38/hg38 4p16.3-12(chr4:36424-47491595)x3	LOC129992145, LOC129992146 +1209 more	Copy number gain	See cases	GPathogenic
Select item 150735	GRCh38/hg38 4p16.3-15.32(chr4:37335-15869056)x1	AFAP1, AFAP1-AS1 +633 more	Copy number loss	See cases	GPathogenic
Select item 146749	GRCh38/hg38 4p16.3-16.1(chr4:37335-9369258)x1	ABLIM2, ACOX3 +504 more	Copy number loss	See cases	GPathogenic
Select item 145401	GRCh38/hg38 4p16.3(chr4:37335-3775112)x1	ADD1, ADRA2C +277 more	Copy number loss	See cases	GPathogenic
Select item 147969	GRCh38/hg38 4p16.3-15.31(chr4:51519-17798196)x3	ABLIM2, ACOX3 +674 more	Copy number gain	See cases	GPathogenic
Select item 57275	GRCh38/hg38 4p16.3(chr4:51519-3775116)x3	ADD1, ADRA2C +277 more	Copy number gain	See cases	GPathogenic
Select item 57239	GRCh38/hg38 4p16.3-16.1(chr4:51519-8222798)x3	ABLIM2, ADD1 +461 more	Copy number gain	See cases	GPathogenic
Select item 57874	GRCh38/hg38 4p16.3-15.33(chr4:56878-14499760)x1	ABLIM2, ACOX3 +597 more	Copy number loss	See cases	GPathogenic
Select item 57873	GRCh38/hg38 4p16.3(chr4:56878-3870653)x1	CTBP1-AS, CTBP1-DT +278 more	Copy number loss	See cases	GPathogenic
Select item 155646	GRCh38/hg38 4p16.3-15.31(chr4:68453-20385608)x1	LOC129992028, LOC129992029 +691 more	Copy number loss	See cases	GPathogenic
Select item 155619	GRCh38/hg38 4p16.3-15.33(chr4:68453-14612453)x1	LOC129992002, LOC129992003 +597 more	Copy number loss	See cases	GPathogenic
Select item 155480	GRCh38/hg38 4p16.3-16.1(chr4:68453-6055026)x1	LOC101928279, LOC101928306 +346 more	Copy number loss	See cases	GPathogenic
Select item 155310	GRCh38/hg38 4p16.3-16.1(chr4:68453-8730129)x1	ABLIM2, ACOX3 +479 more	Copy number loss	See cases	GPathogenic
Select item 155257	GRCh38/hg38 4p16.3(chr4:72555-2689579)x1	LOC129992008, LOC129992009 +175 more	Copy number loss	See cases	GPathogenic
Select item 149255	GRCh38/hg38 4p16.3-15.31(chr4:72555-21022414)x3	LOC126806993, LOC126806994 +702 more	Copy number gain	See cases	GPathogenic
Select item 149142	GRCh38/hg38 4p16.3-15.33(chr4:72555-12898612)x1	ABLIM2, ACOX3 +569 more	Copy number loss	See cases	GPathogenic
Select item 147922	GRCh38/hg38 4p16.3-16.1(chr4:72555-10250666)x1	ABLIM2, ACOX3 +536 more	Copy number loss	See cases	GPathogenic
Select item 147791	GRCh38/hg38 4p16.3(chr4:72555-3724047)x1	ADD1, ATP5ME +274 more	Copy number loss	See cases	GPathogenic
Select item 147686	GRCh38/hg38 4p16.3(chr4:72555-4358718)x1	ATP5ME, CFAP99 +290 more	Copy number loss	See cases	GPathogenic
Select item 147562	GRCh38/hg38 4p16.3(chr4:72555-3561655)x1	ADD1, ATP5ME +271 more	Copy number loss	See cases	GPathogenic
Select item 147376	GRCh38/hg38 4p16.3-16.1(chr4:72555-6243425)x1	ADD1, ADRA2C +363 more	Copy number loss	See cases	GPathogenic
Select item 146353	GRCh38/hg38 4p16.3-15.32(chr4:72555-17278013)x1	ABLIM2, ACOX3 +657 more	Copy number loss	See cases	GPathogenic
Select item 146279	GRCh38/hg38 4p16.3-16.2(chr4:72555-4888108)x1	ADD1, ADRA2C +313 more	Copy number loss	See cases	GPathogenic
Select item 146219	GRCh38/hg38 4p16.3-15.32(chr4:72555-15658035)x1	ABLIM2, ACOX3 +623 more	Copy number loss	See cases	GPathogenic
Select item 144364	GRCh38/hg38 4p16.3-16.2(chr4:72555-5344810)x1	ADD1, ADRA2C +323 more	Copy number loss	See cases	GPathogenic
Select item 144195	GRCh38/hg38 4p16.3-14(chr4:72555-39477144)x3	ABLIM2, ACOX3 +1039 more	Copy number gain	See cases	GPathogenic
Select item 58012	GRCh38/hg38 4p16.3-16.2(chr4:72555-5607083)x3	ADD1, ADRA2C +327 more	Copy number gain	See cases	GPathogenic
Select item 58011	GRCh38/hg38 4p16.3-15.1(chr4:72555-33130620)x3	LOC129992237, LOC129992238 +861 more	Copy number gain	See cases	GPathogenic
Select item 57935	GRCh38/hg38 4p16.3-16.2(chr4:72555-5212384)x1	ADD1, ADRA2C +322 more	Copy number loss	See cases	GPathogenic
Select item 57933	GRCh38/hg38 4p16.3(chr4:72555-3847154)x3	ADD1, ADRA2C +278 more	Copy number gain	See cases	GPathogenic
Select item 57929	GRCh38/hg38 4p16.3-16.2(chr4:72555-5034991)x1	LOC129991980, LOC129991981 +319 more	Copy number loss	See cases	GPathogenic
Select item 57905	GRCh38/hg38 4p16.3(chr4:72555-3206313)x1	ADD1, ATP5ME +249 more	Copy number loss	See cases	GPathogenic
Select item 57904	GRCh38/hg38 4p16.3(chr4:72555-3785385)x1	LOC123466217, LOC123466218 +277 more	Copy number loss	See cases	GPathogenic
Select item 57903	GRCh38/hg38 4p16.3(chr4:72555-2325477)x1	ATP5ME, CPLX1 +152 more	Copy number loss	See cases	GPathogenic
Select item 57902	GRCh38/hg38 4p16.3-15.1(chr4:72555-28066309)x1	LOC129992157, LOC129992158 +832 more	Copy number loss	See cases	GPathogenic
Select item 57901	GRCh38/hg38 4p16.3-16.1(chr4:72555-7829425)x1	NSD2, NSG1 +438 more	Copy number loss	See cases	GPathogenic
Select item 146023	GRCh38/hg38 4p16.3-15.32(chr4:78578-15625573)x3	ABLIM2, ACOX3 +618 more	Copy number gain	See cases	GPathogenic
Select item 146010	GRCh38/hg38 4p16.3-16.1(chr4:78578-10335613)x1	LOC129992049, LOC129992050 +537 more	Copy number loss	See cases	GPathogenic
Select item 145991	GRCh38/hg38 4p16.3(chr4:78578-3363219)x1	LOC129992097, LOC129992098 +256 more	Copy number loss	See cases	GPathogenic
Select item 58015	GRCh38/hg38 4p16.3-14(chr4:85149-38700366)x3	SOD3, SORCS2 +987 more	Copy number gain	See cases	GPathogenic
Select item 58014	GRCh38/hg38 4p16.3-16.2(chr4:85149-4596207)x3	ADD1, ADRA2C +300 more	Copy number gain	See cases	GPathogenic
Select item 58013	GRCh38/hg38 4p16.3-15.2(chr4:85149-22450018)x3	ABLIM2, ACOX3 +716 more	Copy number gain	See cases	GPathogenic
Select item 57939	GRCh38/hg38 4p16.3(chr4:85149-4405782)x1	ADD1, ADRA2C +291 more	Copy number loss	See cases	GPathogenic
Select item 57938	GRCh38/hg38 4p16.3-16.1(chr4:85149-7843616)x1	LOC129992176, LOC129992177 +439 more	Copy number loss	See cases	GPathogenic
Select item 57937	GRCh38/hg38 4p16.3-15.32(chr4:85149-17486742)x1	ABLIM2, ACOX3 +659 more	Copy number loss	See cases	GPathogenic
Select item 57936	GRCh38/hg38 4p16.3-16.1(chr4:85149-7063699)x1	ADD1, ADRA2C +414 more	Copy number loss	See cases	GPathogenic
Select item 2579174	GRCh38/hg38 4p16.3-q12(chr4:85624-57073230)x3	LOC129992561, LOC129992562 +1409 more	Copy number gain	Neurodevelopmental disorder	GPathogenic
Select item 146113	GRCh38/hg38 4p16.3-16.1(chr4:135972-9369341)x1	ABLIM2, ACOX3 +500 more	Copy number loss	See cases	GPathogenic
Select item 57182	GRCh38/hg38 4p16.3(chr4:620566-2958209)x3	LOC129991981, LOC129991982 +206 more	Copy number gain	See cases	GPathogenic
Select item 148893	GRCh38/hg38 4p16.3(chr4:1723429-2286479)x3	FGFR3, HAUS3 +37 more	Copy number gain	See cases	GUncertain significance
Select item 153619	GRCh38/hg38 4p16.3-16.2(chr4:1964539-5912172)x1	ADD1, ADRA2C +216 more	Copy number loss	See cases	GPathogenic
Select item 154242	GRCh38/hg38 4p16.3(chr4:2007739-3078685)x1	ADD1, CFAP99 +118 more	Copy number loss	See cases	GLikely pathogenic
Select item 149071	GRCh38/hg38 4p16.3(chr4:2019774-3881330)x3	ADD1, ADRA2C +149 more	Copy number gain	See cases	GUncertain significance
Select item 2619104	NM_181808.4(POLN):c.128C>T (p.Thr43Ile)	HAUS3, POLN (T43I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484777	NM_181808.4(POLN):c.115T>C (p.Trp39Arg)	HAUS3, POLN (W39R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296432	NM_181808.4(POLN):c.95A>T (p.Asp32Val)	HAUS3, POLN (D32V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234481	NM_181808.4(POLN):c.92G>A (p.Gly31Asp)	HAUS3, POLN (G31D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489982	NM_001303143.2(HAUS3):c.1760T>C (p.Val587Ala)	HAUS3, POLN (V587A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300811	NM_001303143.2(HAUS3):c.1759G>A (p.Val587Met)	HAUS3, POLN (V587M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2689195	NM_001303143.2(HAUS3):c.1679T>C (p.Leu560Ser)	HAUS3, POLN (L560S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3104323	NM_001303143.2(HAUS3):c.1678T>G (p.Leu560Val)	HAUS3, POLN (L560V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204042	NM_001303143.2(HAUS3):c.1553G>A (p.Gly518Glu)	HAUS3, POLN (G518E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553752	NM_001303143.2(HAUS3):c.1513A>G (p.Lys505Glu)	HAUS3, POLN (K505E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104322	NM_001303143.2(HAUS3):c.1494C>A (p.Phe498Leu)	HAUS3, POLN (F498L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279553	NM_001303143.2(HAUS3):c.1369G>A (p.Gly457Arg)	HAUS3, POLN (G457R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363750	NM_001303143.2(HAUS3):c.1333G>A (p.Asp445Asn)	HAUS3, POLN (D445N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283528	NM_001303143.2(HAUS3):c.1319C>A (p.Thr440Asn)	HAUS3, POLN (T440N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104321	NM_001303143.2(HAUS3):c.1303A>G (p.Ile435Val)	HAUS3, POLN (I435V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283524	NM_001303143.2(HAUS3):c.1275G>A (p.Met425Ile)	HAUS3, POLN (M425I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2266682	NM_001303143.2(HAUS3):c.1250T>G (p.Met417Arg)	HAUS3, POLN (M417R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374831	NM_001303143.2(HAUS3):c.1229A>G (p.Gln410Arg)	HAUS3, POLN (Q410R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545458	NM_001303143.2(HAUS3):c.1208G>T (p.Arg403Leu)	HAUS3, POLN (R403L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354642	NM_001303143.2(HAUS3):c.1003A>G (p.Ser335Gly)	HAUS3, POLN (S335G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393887	NM_001303143.2(HAUS3):c.946A>G (p.Ser316Gly)	HAUS3, POLN (S316G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104327	NM_001303143.2(HAUS3):c.944C>G (p.Ser315Cys)	HAUS3, POLN (S315C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316190	NM_001303143.2(HAUS3):c.940A>T (p.Ile314Phe)	HAUS3, POLN (I314F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520633	NM_001303143.2(HAUS3):c.808A>G (p.Ile270Val)	HAUS3, POLN (I270V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104326	NM_001303143.2(HAUS3):c.797A>G (p.Gln266Arg)	HAUS3, POLN (Q266R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364784	NM_001303143.2(HAUS3):c.779T>C (p.Leu260Pro)	HAUS3, POLN (L260P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104325	NM_001303143.2(HAUS3):c.776G>A (p.Arg259Gln)	HAUS3, POLN (R259Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516081	NM_001303143.2(HAUS3):c.704A>G (p.Glu235Gly)	HAUS3, POLN (E235G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520799	NM_001303143.2(HAUS3):c.660A>T (p.Lys220Asn)	HAUS3, POLN (K220N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558009	NM_001303143.2(HAUS3):c.635C>T (p.Ala212Val)	HAUS3, POLN (A212V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283523	NM_001303143.2(HAUS3):c.544C>G (p.His182Asp)	HAUS3, POLN (H182D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283529	NM_001303143.2(HAUS3):c.509C>G (p.Thr170Ser)	HAUS3, POLN (T170S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283521	NM_001303143.2(HAUS3):c.491A>G (p.Asn164Ser)	HAUS3, POLN (N164S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283526	NM_001303143.2(HAUS3):c.441G>T (p.Lys147Asn)	HAUS3, POLN (K147N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219950	NM_001303143.2(HAUS3):c.434C>T (p.Thr145Ile)	HAUS3, POLN (T145I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386799	NM_001303143.2(HAUS3):c.428A>C (p.Glu143Ala)	HAUS3, POLN (E143A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410016	NM_001303143.2(HAUS3):c.359G>T (p.Arg120Leu)	HAUS3, POLN (R120L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213282	NM_001303143.2(HAUS3):c.351T>G (p.Ile117Met)	HAUS3, POLN (I117M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283522	NM_001303143.2(HAUS3):c.343C>G (p.Leu115Val)	HAUS3, POLN (L115V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254973	NM_001303143.2(HAUS3):c.298G>A (p.Glu100Lys)	HAUS3, POLN (E100K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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