RNF212[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 155150	GRCh38/hg38 4p16.3(chr4:36424-1562150)x1	ATP5ME, CPLX1 +91 more	Copy number loss	See cases	GUncertain significance
Select item 155105	GRCh38/hg38 4p16.3(chr4:36424-1956092)x1	SLC49A3, SPON2 +124 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 148311	GRCh38/hg38 4p16.3(chr4:36424-1581567)x3	ATP5ME, CPLX1 +95 more	Copy number gain	See cases	GLikely pathogenic
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 147744	GRCh38/hg38 4p16.3(chr4:51519-1405362)x1	ATP5ME, CPLX1 +90 more	Copy number loss	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 57898	GRCh38/hg38 4p16.3(chr4:56878-2213205)x1	LOC129991962, LOC129991963 +137 more	Copy number loss	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 153530	GRCh38/hg38 4p16.3(chr4:68453-1997458)x1	ATP5ME, CPLX1 +127 more	Copy number loss	See cases	GPathogenic
Select item 161057	GRCh38/hg38 4p16.3(chr4:72555-2108607)x1	ATP5ME, CPLX1 +134 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 150613	GRCh38/hg38 4p16.3(chr4:72555-1581567)x1	ATP5ME, CPLX1 +95 more	Copy number loss	See cases	GUncertain significance
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 148049	GRCh38/hg38 4p16.3(chr4:72555-1153038)x1	ATP5ME, CPLX1 +58 more	Copy number loss	See cases	GUncertain significance
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 57823	GRCh38/hg38 4p16.3(chr4:72555-1405362)x3	ATP5ME, CPLX1 +90 more	Copy number gain	See cases	GUncertain significance
Select item 57159	GRCh38/hg38 4p16.3(chr4:72555-2108607)x1	ATP5ME, CPLX1 +134 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 59418	GRCh38/hg38 4p16.3(chr4:85149-2008535)x1	ATP5ME, CPLX1 +127 more	Copy number loss	See cases	GPathogenic
Select item 59417	GRCh38/hg38 4p16.3(chr4:85149-1919505)x1	ATP5ME, CPLX1 +124 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 59419	GRCh38/hg38 4p16.3(chr4:336191-2213205)x1	ATP5ME, CPLX1 +131 more	Copy number loss	See cases	GPathogenic
Select item 146344	GRCh38/hg38 4p16.3(chr4:620566-1405362)x3	ATP5ME, CPLX1 +72 more	Copy number gain	See cases	GUncertain significance
Select item 57182	GRCh38/hg38 4p16.3(chr4:620566-2958209)x3	LOC129991981, LOC129991982 +206 more	Copy number gain	See cases	GPathogenic
Select item 3030160	NM_001366918.1(RNF212):c.*2G>C	RNF212	Single nucleotide variant (3 prime UTR variant)	RNF212-related disorder	GLikely benign
Select item 3043676	NM_001366919.1(RNF212):c.814+10C>T	RNF212	Single nucleotide variant (intron variant)	RNF212-related disorder	GLikely benign
Select item 3029674	NM_001366919.1(RNF212):c.807G>A (p.Gln269=)	RNF212	Single nucleotide variant (synonymous variant +1 more)	RNF212-related disorder	GLikely benign
Select item 3031982	NM_001366919.1(RNF212):c.804G>A (p.Arg268=)	RNF212	Single nucleotide variant (synonymous variant +1 more)	RNF212-related disorder	GBenign
Select item 3047718	NM_001366919.1(RNF212):c.787C>T (p.Pro263Ser)	RNF212 (P263S)	Single nucleotide variant (missense variant +1 more)	RNF212-related disorder	GBenign
Select item 3033074	NM_001366918.1(RNF212):c.647+9_647+37del	RNF212	Deletion (intron variant)	RNF212-related disorder	GLikely benign
Select item 3032404	NM_001366918.1(RNF212):c.647+9C>T	RNF212	Single nucleotide variant (intron variant)	RNF212-related disorder	GLikely benign
Select item 3046854	NM_001366918.1(RNF212):c.631A>G (p.Met211Val)	RNF212 (M211V)	Single nucleotide variant (missense variant)	RNF212-related disorder	GBenign
Select item 3047327	NM_001366918.1(RNF212):c.590T>G (p.Leu197Arg)	RNF212 (L197R)	Single nucleotide variant (missense variant)	RNF212-related disorder	GBenign
Select item 3314844	NM_001131034.4(RNF212):c.863T>C (p.Leu288Pro)	RNF212 (L288P)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2278294	NM_001131034.4(RNF212):c.752A>T (p.Lys251Ile)	RNF212 (K251I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3155288	NM_001131034.4(RNF212):c.714G>A (p.Ala238=)	RNF212 (V221I)	Single nucleotide variant (synonymous variant +3 more)	not specified	GLikely benign
Select item 3314843	NM_001131034.4(RNF212):c.689G>A (p.Cys230Tyr)	RNF212 (C230Y)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3155287	NM_001131034.4(RNF212):c.621G>T (p.Leu207Phe)	RNF212 (L207F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3155286	NM_001131034.4(RNF212):c.616A>C (p.Thr206Pro)	RNF212 (T206P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2564890	NM_001131034.4(RNF212):c.553C>T (p.Pro185Ser)	RNF212 (P185S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155285	NM_001131034.4(RNF212):c.401A>G (p.Lys134Arg)	RNF212 (K134R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 736	NM_001131034.4(RNF212):c.362+1497C>T	RNF212	Single nucleotide variant (intron variant)	Recombination rate quantitative trait locus 1	Gassociation
Select item 2207921	NM_001131034.4(RNF212):c.347T>C (p.Ile116Thr)	RNF212 (I116T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 221323	NM_001131034.4(RNF212):c.314T>C (p.Leu105Ser)	RNF212 (L105S)	Single nucleotide variant (missense variant +1 more)	Breast ductal adenocarcinoma	GUncertain significance
Select item 1222937	NM_001131034.4(RNF212):c.247-2639A>G	RNF212 (I262V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1244231	NM_001131034.4(RNF212):c.247-2703_247-2702del	RNF212 (R240fs)	Deletion (frameshift variant +1 more)	Non-obstructive azoospermia	GUncertain significance
Select item 403382	NM_001131034.4(RNF212):c.247-2861C>T	RNF212 (Q188*)	Single nucleotide variant (nonsense +1 more)	not specified	GBenign
Select item 2346423	NM_001131034.4(RNF212):c.207A>G (p.Ile69Met)	RNF212 (I69M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535759	NM_001131034.4(RNF212):c.200T>C (p.Met67Thr)	RNF212 (M67T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544929	NM_001131034.4(RNF212):c.179C>T (p.Ala60Val)	RNF212 (A60V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 735	NM_001131034.4(RNF212):c.172-4654T>C	RNF212	Single nucleotide variant (intron variant)	Recombination rate quantitative trait locus 1	Gassociation
Select item 2469565	NM_001131034.4(RNF212):c.170A>T (p.His57Leu)	RNF212 (H57L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324689	NM_001131034.4(RNF212):c.152C>T (p.Thr51Ile)	RNF212 (T51I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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