ClinVar for Gene (Select 140432) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314682	NM_178861.5(RNF113B):c.311G>A (p.Gly104Glu)	FARP1, RNF113B (G104E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314681	NM_178861.5(RNF113B):c.577C>T (p.Pro193Ser)	FARP1, RNF113B (P193S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154958	NM_178861.5(RNF113B):c.962A>C (p.Lys321Thr)	FARP1, RNF113B (K321T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154957	NM_178861.5(RNF113B):c.886C>T (p.Pro296Ser)	FARP1, RNF113B (P296S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3154956	NM_178861.5(RNF113B):c.563G>A (p.Arg188His)	FARP1, RNF113B (R188H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154955	NM_178861.5(RNF113B):c.536C>G (p.Ala179Gly)	FARP1, RNF113B (A179G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154953	NM_178861.5(RNF113B):c.355G>A (p.Glu119Lys)	FARP1, RNF113B (E119K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154952	NM_178861.5(RNF113B):c.271G>A (p.Asp91Asn)	FARP1, RNF113B (D91N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154951	NM_178861.5(RNF113B):c.251A>C (p.Glu84Ala)	FARP1, RNF113B (E84A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154950	NM_178861.5(RNF113B):c.176C>G (p.Pro59Arg)	FARP1, RNF113B (P59R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3148881	GRCh37/hg19 13q32.2-33.3(chr13:98773859-109277603)x1	ABHD13, ARGLU1 +34 more	Copy number loss	not provided	GPathogenic
Select item 3063309	GRCh37/hg19 13q31.1-34(chr13:84669397-115107733)x1	ABCC4, ABHD13 +97 more	Copy number loss	not specified	GPathogenic
Select item 3063294	GRCh37/hg19 13q31.1-34(chr13:82876219-115107733)x3	ABCC4, ABHD13 +98 more	Copy number gain	not specified	GPathogenic
Select item 3063280	GRCh37/hg19 13q21.31-33.1(chr13:64825656-103641349)x1	ABCC4, ACOD1 +81 more	Copy number loss	not specified	GPathogenic
Select item 2685478	GRCh37/hg19 13q31.2-33.2(chr13:89012420-106371634)x1	PCCA, POGLUT2 +50 more	Copy number loss	not provided	GPathogenic
Select item 2685475	GRCh37/hg19 13q31.1-34(chr13:82131211-115107733)x1	ANKRD10, ANKRD10-IT1 +98 more	Copy number loss	not provided	GPathogenic
Select item 2685473	GRCh37/hg19 13q21.33-33.1(chr13:73132193-104595598)x1	ABCC4, ACOD1 +78 more	Copy number loss	not provided	GPathogenic
Select item 2684705	GRCh37/hg19 13q22.1-34(chr13:73488238-115107733)x3	GPR18, GRTP1 +121 more	Copy number gain	not provided	GPathogenic
Select item 2684703	GRCh37/hg19 13q21.2-34(chr13:61534068-115107733)x3	TBC1D4, TEX29 +129 more	Copy number gain	not provided	GPathogenic
Select item 2591517	NM_178861.5(RNF113B):c.506C>T (p.Ser169Leu)	FARP1, RNF113B (S169L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559328	NM_178861.5(RNF113B):c.79C>T (p.Arg27Trp)	FARP1, RNF113B (R27W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541598	NM_178861.5(RNF113B):c.103A>G (p.Lys35Glu)	FARP1, RNF113B (K35E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520858	NM_178861.5(RNF113B):c.293G>A (p.Arg98His)	FARP1, RNF113B (R98H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514305	NM_178861.5(RNF113B):c.4G>C (p.Ala2Pro)	FARP1, RNF113B (A2P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484267	NM_178861.5(RNF113B):c.231C>A (p.His77Gln)	FARP1, RNF113B (H77Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482219	NM_178861.5(RNF113B):c.863C>T (p.Pro288Leu)	FARP1, RNF113B (P288L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477215	NM_178861.5(RNF113B):c.133G>A (p.Glu45Lys)	FARP1, RNF113B (E45K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2446726	GRCh37/hg19 13q32.1-33.2(chr13:95700999-105271065)x3	DZIP1, ERCC5 +35 more	Copy number gain	See cases	GPathogenic
Select item 2398683	NM_178861.5(RNF113B):c.742G>A (p.Glu248Lys)	FARP1, RNF113B (E248K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397214	NM_178861.5(RNF113B):c.361G>A (p.Glu121Lys)	FARP1, RNF113B (E121K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334329	NM_178861.5(RNF113B):c.292C>T (p.Arg98Cys)	FARP1, RNF113B (R98C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2310142	NM_178861.5(RNF113B):c.456C>G (p.Ser152Arg)	FARP1, RNF113B (S152R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291962	NM_178861.5(RNF113B):c.80G>T (p.Arg27Leu)	FARP1, RNF113B (R27L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286453	NM_178861.5(RNF113B):c.107G>A (p.Arg36His)	FARP1, RNF113B (R36H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277972	NM_178861.5(RNF113B):c.40G>A (p.Ala14Thr)	FARP1, RNF113B (A14T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266074	NM_178861.5(RNF113B):c.887C>T (p.Pro296Leu)	FARP1, RNF113B (P296L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254375	NM_178861.5(RNF113B):c.646G>A (p.Asp216Asn)	FARP1, RNF113B (D216N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1809091	GRCh37/hg19 13q32.2(chr13:98720234-99172213)x3	FARP1, RNF113B +1 more	Copy number gain	not provided	GUncertain significance
Select item 1808983	GRCh37/hg19 13q32.1-34(chr13:97142120-115107733)x1	ABHD13, ADPRHL1 +76 more	Copy number loss	not provided	GPathogenic
Select item 1808883	GRCh37/hg19 13q32.2(chr13:98654981-98914693)x3	FARP1, IPO5 +1 more	Copy number gain	not provided	GUncertain significance
Select item 1808298	GRCh37/hg19 13q32.2(chr13:98514680-98941974)x3	FARP1, IPO5 +1 more	Copy number gain	not provided	GUncertain significance
Select item 1808276	GRCh37/hg19 13q31.3-33.2(chr13:93535335-105788229)x1	BIVM-ERCC5, CCDC168 +40 more	Copy number loss	not provided	GPathogenic
Select item 1807731	GRCh37/hg19 13q22.1-34(chr13:75268539-115107733)x3	ABCC4, ABHD13 +116 more	Copy number gain	not provided	GPathogenic
Select item 1710518	GRCh37/hg19 13q11-34(chr13:19253848-115108937)x3	B3GLCT, HS6ST3 +332 more	Copy number gain	not provided	GPathogenic
Select item 1707439	GRCh37/hg19 13q31.2-34(chr13:89490345-115062235)x3	ABCC4, ABHD13 +93 more	Copy number gain	See cases	GPathogenic
Select item 1703573	GRCh37/hg19 13p13-q34(chr13:1-115169878)	ABCC4, ABHD13 +332 more	Copy number gain	Complete trisomy 13 syndrome	GPathogenic
Select item 1527790	GRCh37/hg19 13q32.1-32.3(chr13:95677119-100521192)	ABCC4, CLDN10 +18 more	Copy number loss	not specified	GUncertain significance
Select item 1527788	GRCh37/hg19 13q31.2-34(chr13:88073140-115107733)	ABCC4, ABHD13 +96 more	Copy number loss	not specified	GPathogenic
Select item 1527787	GRCh37/hg19 13q31.1-34(chr13:85037147-115107733)	ABCC4, ABHD13 +97 more	Copy number gain	not specified	GPathogenic
Select item 1527786	GRCh37/hg19 13q31.1-34(chr13:79370012-115107733)	DCUN1D2, ERCC5 +101 more	Copy number loss	not specified	GPathogenic
Select item 1527785	GRCh37/hg19 13q22.3-34(chr13:78514567-115107733)	MIR18A, MIR19A +104 more	Copy number gain	not specified	GPathogenic
Select item 1527777	GRCh37/hg19 13q21.2-34(chr13:61424168-115107733)	ACOD1, ADPRHL1 +129 more	Copy number gain	not specified	GPathogenic
Select item 1527750	GRCh37/hg19 13q11-34(chr13:19436286-115107733)	ABCC4, ABHD13 +332 more	Copy number gain	not specified	GPathogenic
Select item 1527749	GRCh37/hg19 13q11-34(chr13:19436286-114981726)	VPS36, VWA8 +329 more	Copy number gain	not specified	GPathogenic
Select item 1341277	GRCh37/hg19 13q14.11-33.3(chr13:42504540-108206269)x3	GTF2F2, PRR20D +175 more	Copy number gain	not provided	GPathogenic
Select item 1341081	GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	ABCC4, ABHD13 +332 more	Copy number gain	not provided	GPathogenic
Select item 1321996	GRCh37/hg19 13p13-q34(chr13:1-115169878)x3	DACH1, IRS2 +332 more	Copy number gain	See cases	GPathogenic
Select item 1077192	Single allele	ITGBL1, LIG4 +58 more	Deletion	Distal monosomy 13q	GPathogenic
Select item 1074668	NC_000013.10:g.(?_92002837)_(103343314_?)del	ABCC4, CLDN10 +41 more	Deletion	Holoprosencephaly 5	GPathogenic
Select item 1048617	GRCh37/hg19 13q11-34(chr13:19053605-115108528)x3	CENPJ, CHAMP1 +332 more	Copy number gain	See cases	GPathogenic
Select item 815614	GRCh37/hg19 13q32.1-34(chr13:96895656-115107733)x1	ABHD13, ADPRHL1 +76 more	Copy number loss	not provided	GPathogenic
Select item 815612	GRCh37/hg19 13q32.1-33.2(chr13:96240346-106103782)x1	BIVM, BIVM-ERCC5 +33 more	Copy number loss	not provided	GPathogenic
Select item 815590	GRCh37/hg19 13q14.3-34(chr13:53262013-115107733)x1	CDC16, NALCN +142 more	Copy number loss	not provided	GPathogenic
Select item 688438	GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	ABCC4, ABHD13 +332 more	Copy number gain	not provided	GPathogenic
Select item 687326	GRCh37/hg19 13q21.2-34(chr13:61775567-115107733)x3	ABCC4, ABHD13 +129 more	Copy number gain	not provided	GPathogenic
Select item 687002	GRCh37/hg19 13q31.3-34(chr13:94849303-115107733)x3	ABCC4, ABHD13 +86 more	Copy number gain	not provided	GUncertain significance
Select item 686204	GRCh37/hg19 13q32.2(chr13:98659899-98908125)x3	FARP1, IPO5 +1 more	Copy number gain	not provided	GUncertain significance
Select item 564082	GRCh37/hg19 13q22.3-34(chr13:78590089-115107733)x3	ABCC4, ABHD13 +103 more	Copy number gain	not provided	GPathogenic
Select item 564081	GRCh37/hg19 13q31.3-33.3(chr13:94703767-109731879)x1	ABCC4, ABHD13 +49 more	Copy number loss	not provided	GPathogenic
Select item 443213	GRCh37/hg19 13q31.1-34(chr13:83435292-115107733)x3	ABCC4, ABHD13 +98 more	Copy number gain	See cases	GPathogenic
Select item 443022	GRCh37/hg19 13q32.2-33.1(chr13:98607855-104370539)x3	BIVM, BIVM-ERCC5 +26 more	Copy number gain	See cases	GLikely pathogenic
Select item 442938	GRCh37/hg19 13q32.1-34(chr13:96586481-115107733)x1	ABHD13, ADPRHL1 +77 more	Copy number loss	See cases	GPathogenic
Select item 442796	GRCh37/hg19 13q21.1-34(chr13:56431743-115107733)	ABCC4, ABHD13 +137 more	Copy number gain	See cases	GPathogenic
Select item 442647	GRCh37/hg19 13q31.3-34(chr13:94474530-115107733)x1	ABCC4, ABHD13 +86 more	Copy number loss	See cases	GPathogenic
Select item 442644	GRCh37/hg19 13q32.1-33.1(chr13:98158452-101950563)x3	RNF113B, SLC15A1 +15 more	Copy number gain	See cases	GLikely pathogenic
Select item 442311	GRCh37/hg19 13q31.1-34(chr13:85176519-115107733)x3	TGDS, TM9SF2 +97 more	Copy number gain	See cases	GPathogenic
Select item 441797	GRCh37/hg19 13q31.1-34(chr13:80058840-115107733)x3	ABCC4, ABHD13 +100 more	Copy number gain	See cases	GPathogenic
Select item 441765	GRCh37/hg19 13q11-34(chr13:19436287-115107733)	FGF9, FLT1 +332 more	Copy number gain	See cases	GPathogenic
Select item 441764	GRCh37/hg19 13q11-34(chr13:19436287-115107733)x3	ABCC4, ABHD13 +332 more	Copy number gain	See cases	GPathogenic
Select item 441737	GRCh37/hg19 13q31.1-33.3(chr13:80572498-108719528)x1	ABCC4, ARGLU1 +58 more	Copy number loss	See cases	GPathogenic
Select item 441662	GRCh37/hg19 13q21.33-34(chr13:71871468-115107733)x4	ABCC4, ABHD13 +125 more	Copy number gain	See cases	GPathogenic
Select item 395478	GRCh37/hg19 13q14.3-33.3(chr13:53551300-109850651)x1	MIR4500HG, MIR92A1 +102 more	Copy number loss	See cases	GPathogenic
Select item 395197	GRCh37/hg19 13q31.1-33.1(chr13:81851091-102864674)x1	ABCC4, CLDN10 +43 more	Copy number loss	See cases	GPathogenic
Select item 395156	GRCh37/hg19 13q31.1-34(chr13:82221361-115092569)x3	ABCC4, ABHD13 +98 more	Copy number gain	See cases	GPathogenic
Select item 394462	GRCh37/hg19 13q12.11-34(chr13:19571503-115092510)	CRYL1, CSNK1A1L +332 more	Copy number gain	See cases	GPathogenic
Select item 253491	GRCh37/hg19 13q31.2-34(chr13:89796110-115083342)x1	ABCC4, ABHD13 +94 more	Copy number loss	See cases	GPathogenic
Select item 253405	GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	GTF2F2, LINC00567 +332 more	Copy number gain	See cases	GPathogenic
Select item 160881	GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3	LOC126861859, LOC126861860 +2025 more	Copy number gain	See cases	GPathogenic
Select item 155395	GRCh38/hg38 13q11-34(chr13:18862146-114342258)x3	ABCC4, ABHD13 +2046 more	Copy number gain	See cases	GPathogenic
Select item 154857	GRCh38/hg38 13q12.11-34(chr13:19671934-114340331)x3	LOC130009607, LOC130009608 +2029 more	Copy number gain	See cases	GPathogenic
Select item 153403	GRCh38/hg38 13q31.1-34(chr13:83288131-114342258)x3	ABCC4, ABHD13 +663 more	Copy number gain	See cases	GPathogenic
Select item 152729	GRCh38/hg38 13q31.1-34(chr13:78964223-114340331)x3	LOC124946344, LOC124946345 +706 more	Copy number gain	See cases	GPathogenic
Select item 151282	GRCh38/hg38 13q11-34(chr13:18456040-114340285)x3	LOC130009892, LOC130009893 +2050 more	Copy number gain	See cases	GPathogenic
Select item 150277	GRCh38/hg38 13q32.1-34(chr13:96745059-114327106)x3	DOCK9-DT, EFNB2 +544 more	Copy number gain	See cases	GPathogenic
Select item 150189	GRCh38/hg38 13q12.11-34(chr13:19833130-114327106)x3	ABCC4, ABHD13 +2025 more	Copy number gain	See cases	GPathogenic
Select item 150153	GRCh38/hg38 13q31.2-32.3(chr13:87944479-99866542)x1	LOC130010040, LOC130010041 +236 more	Copy number loss	See cases	GPathogenic
Select item 150125	GRCh38/hg38 13q32.1-34(chr13:95744855-110863818)x3	LOC130010039, LOC130010040 +369 more	Copy number gain	See cases	GPathogenic
Select item 149780	GRCh38/hg38 13q31.1-34(chr13:78999318-114327106)x3	LOC130010101, LOC130010102 +705 more	Copy number gain	See cases	GPathogenic
Select item 149290	GRCh38/hg38 13q31.1-34(chr13:86788927-114340331)x1	ABCC4, ABHD13 +650 more	Copy number loss	See cases	GPathogenic
Select item 148962	GRCh38/hg38 13q32.1-33.3(chr13:97213871-109162916)x1	LOC124946325, LOC124946326 +271 more	Copy number loss	See cases	GPathogenic

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