ClinVar for Gene (Select 64108) - ClinVar

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Links from Gene

Items: 55

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3315737	NM_022147.3(RTP4):c.204G>C (p.Gln68His)	RTP4 (Q68H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315736	NM_022147.3(RTP4):c.292T>A (p.Trp98Arg)	RTP4 (W98R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315735	NM_022147.3(RTP4):c.179G>A (p.Arg60Gln)	RTP4 (R60Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315734	NM_022147.3(RTP4):c.47T>A (p.Ile16Asn)	LOC129938132, RTP4 (I16N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157092	NM_022147.3(RTP4):c.65G>T (p.Arg22Leu)	LOC129938132, RTP4 (R22L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157091	NM_022147.3(RTP4):c.440G>T (p.Gly147Val)	RTP4 (G147V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157090	NM_022147.3(RTP4):c.304G>A (p.Glu102Lys)	RTP4 (E102K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157089	NM_022147.3(RTP4):c.287G>A (p.Cys96Tyr)	RTP4 (C96Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157088	NM_022147.3(RTP4):c.273A>C (p.Gln91His)	RTP4 (Q91H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157087	NM_022147.3(RTP4):c.266T>G (p.Phe89Cys)	RTP4 (F89C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3148910	GRCh37/hg19 3q26.33-29(chr3:179313373-197851444)x3	ABCC5, ABCF3 +136 more	Copy number gain	See cases	GPathogenic
Select item 2671619	Single allele	ABCC5, ABCF3 +145 more	Duplication	not provided	GPathogenic
Select item 2671595	Single allele	MUC20, MUC4 +286 more	Duplication	not provided	GPathogenic
Select item 2544507	NM_022147.3(RTP4):c.50A>G (p.Gln17Arg)	LOC129938132, RTP4 (Q17R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540027	NM_022147.3(RTP4):c.511A>G (p.Thr171Ala)	RTP4 (T171A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532511	NM_022147.3(RTP4):c.710T>A (p.Phe237Tyr)	RTP4 (F237Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480682	NM_022147.3(RTP4):c.307A>G (p.Met103Val)	RTP4 (M103V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410486	NM_022147.3(RTP4):c.64C>T (p.Arg22Trp)	LOC129938132, RTP4 (R22W)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2376283	NM_022147.3(RTP4):c.170C>G (p.Ser57Cys)	RTP4 (S57C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809046	GRCh37/hg19 3q27.1-28(chr3:184170962-188047867)x1	ADIPOQ, AHSG +32 more	Copy number loss	not provided	GLikely pathogenic
Select item 1707630	GRCh37/hg19 3q26.31-29(chr3:171558472-197871052)x3	CCDC50, MELTF +155 more	Copy number gain	Isolated anorectal malformation	GLikely pathogenic
Select item 1707428	GRCh37/hg19 3q27.1-29(chr3:183498520-197851986)x3	ABCC5, ABCF3 +118 more	Copy number gain	See cases	GPathogenic
Select item 1703654	GRCh37/hg19 3q27.1-28(chr3:183556940-188083060)	ABCC5, ABCF3 +53 more	Copy number loss	Short stature	GPathogenic
Select item 1527061	GRCh37/hg19 3q26.33-27.3(chr3:182189525-187212935)	ABCC5, ABCF3 +59 more	Copy number loss	not specified	GPathogenic
Select item 1340189	GRCh37/hg19 3q27.3(chr3:186830759-187192352)x3	MASP1, RPL39L +2 more	Copy number gain	not provided	GUncertain significance
Select item 1328104	GRCh37/hg19 3q26.31-27.3(chr3:175119199-187592480)x3	ABCC5, ABCF3 +82 more	Copy number gain	not provided	GPathogenic
Select item 814507	GRCh37/hg19 3q27.2-27.3(chr3:185879162-187446035)x1	ST6GAL1, DNAJB11 +19 more	Copy number loss	not provided	GPathogenic
Select item 814497	GRCh37/hg19 3q26.2-28(chr3:169617690-190593854)x3	FXR1, HTR3D +113 more	Copy number gain	not provided	GPathogenic
Select item 562853	GRCh37/hg19 3q27.3(chr3:187014693-187137909)x4	RTP4	Copy number gain	not provided	GLikely benign
Select item 562852	GRCh37/hg19 3q27.3-29(chr3:186374365-197851986)x3	PCYT1A, TNK2-AS1 +77 more	Copy number gain	not provided	GPathogenic
Select item 562850	GRCh37/hg19 3q27.1-29(chr3:184003967-197851986)x3	FYTTD1, FAM43A +103 more	Copy number gain	not provided	GPathogenic
Select item 562848	GRCh37/hg19 3q26.33-28(chr3:182650681-191275809)x1	KNG1, FETUB +75 more	Copy number loss	not provided	GPathogenic
Select item 562847	GRCh37/hg19 3q26.33-29(chr3:182539234-197851986)x3	PPP1R2, TBCCD1 +126 more	Copy number gain	not provided	GPathogenic
Select item 545290	NC_000003.12:g.(?_187222939)_(194312782_?)del	ATP13A4, ATP13A4-AS1 +180 more	Deletion	Schizophrenia	GLikely pathogenic
Select item 523279	GRCh37/hg19 3q27.1-28(chr3:184300169-188285627)	FETUB, HRG +32 more	Copy number loss	Cognitive impairment +1 more	GPathogenic
Select item 442401	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	HHLA2, HIGD1A +1054 more	Copy number gain	See cases	GPathogenic
Select item 442400	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	A4GNT, AADAC +1054 more	Copy number gain	See cases	GPathogenic
Select item 393885	GRCh37/hg19 3q25.32-29(chr3:158980631-197766890)x3	ABCC5, ABCF3 +198 more	Copy number gain	See cases	GPathogenic
Select item 253655	GRCh37/hg19 3q27.3-28(chr3:186291045-191037240)x1	GMNC, UTS2B +28 more	Copy number loss	See cases	GPathogenic
Select item 253377	GRCh37/hg19 3q24-29(chr3:142995020-192997215)x4	AADAC, AADACL2 +220 more	Copy number gain	See cases	GPathogenic
Select item 155627	GRCh38/hg38 3q26.1-29(chr3:166137209-198125115)x3	LOC129938260, LOC129938261 +1064 more	Copy number gain	See cases	GPathogenic
Select item 154213	GRCh38/hg38 3q25.31-29(chr3:156118441-198125115)x3	LOC108281160, LOC108281177 +1247 more	Copy number gain	See cases	GPathogenic
Select item 153893	GRCh38/hg38 3q26.1-28(chr3:167717962-188365272)x3	ABCC5, ABCC5-AS1 +627 more	Copy number gain	See cases	GLikely pathogenic
Select item 153734	GRCh38/hg38 3q26.33-28(chr3:181138664-192512023)x1	ABCC5, ABCC5-AS1 +399 more	Copy number loss	See cases	GPathogenic
Select item 152257	GRCh38/hg38 3q25.31-29(chr3:156321878-198113452)x3	ABCC5, ABCC5-AS1 +1245 more	Copy number gain	See cases	GPathogenic
Select item 150609	GRCh38/hg38 3q25.1-29(chr3:152100512-198118383)x3	LOC129938169, LOC129938170 +1318 more	Copy number gain	See cases	GPathogenic
Select item 150107	GRCh38/hg38 3q27.2-27.3(chr3:184843627-187461008)x3	ADIPOQ, ADIPOQ-AS1 +131 more	Copy number gain	See cases	GPathogenic
Select item 149685	GRCh38/hg38 3q26.32-29(chr3:176168525-198118383)x3	ZMAT3, ZNF639 +867 more	Copy number gain	See cases	GPathogenic
Select item 148947	GRCh38/hg38 3q26.32-29(chr3:176439911-198118383)x3	LOC129938282, LOC129938283 +866 more	Copy number gain	See cases	GPathogenic
Select item 148900	GRCh38/hg38 3q27.3-29(chr3:186765148-194409416)x1	ADIPOQ, ADIPOQ-AS1 +237 more	Copy number loss	See cases	GPathogenic
Select item 148012	GRCh38/hg38 3q26.2-29(chr3:168167568-198110178)x3	LOC129938077, LOC129938078 +1041 more	Copy number gain	See cases	GPathogenic
Select item 145614	GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3	LOC115995524, LOC115995525 +2647 more	Copy number gain	See cases	GPathogenic
Select item 57984	GRCh38/hg38 3q25.31-29(chr3:157293378-198134727)x3	LOC132088897, LOC132088898 +1201 more	Copy number gain	See cases	GPathogenic
Select item 57983	GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3	LOC123453201, LOC123453202 +1450 more	Copy number gain	See cases	GPathogenic
Select item 57868	GRCh38/hg38 3q27.2-29(chr3:185485849-198110178)x1	MIR944, MUC20 +557 more	Copy number loss	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 55