ClinVar for Gene (Select 57512) - ClinVar

Links from Gene

Items: 91

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282298	NM_020752.3(GPR158):c.2450C>A (p.Ser817Tyr)	GPR158 (S817Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282297	NM_020752.3(GPR158):c.1741A>G (p.Met581Val)	GPR158 (M581V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282296	NM_020752.3(GPR158):c.1952C>T (p.Thr651Ile)	GPR158 (T651I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282295	NM_020752.3(GPR158):c.1276C>G (p.Leu426Val)	GPR158 (L426V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282294	NM_020752.3(GPR158):c.755G>T (p.Arg252Leu)	GPR158, GPR158-AS1 (R252L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3282293	NM_020752.3(GPR158):c.301G>A (p.Gly101Ser)	GPR158, GPR158-AS1 (G101S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3282292	NM_020752.3(GPR158):c.368A>G (p.His123Arg)	GPR158, GPR158-AS1 (H123R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3282290	NM_020752.3(GPR158):c.107G>C (p.Arg36Pro)	GPR158, GPR158-AS1 (R36P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282289	NM_020752.3(GPR158):c.1439G>A (p.Arg480His)	GPR158 (R480H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282288	NM_020752.3(GPR158):c.2161C>T (p.Leu721Phe)	GPR158 (L721F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282287	NM_020752.3(GPR158):c.1654T>A (p.Leu552Met)	GPR158 (L552M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282286	NM_020752.3(GPR158):c.328G>T (p.Gly110Trp)	GPR158, GPR158-AS1 (G110W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3101569	NM_020752.3(GPR158):c.800C>T (p.Pro267Leu)	GPR158, GPR158-AS1 (P267L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3101568	NM_020752.3(GPR158):c.412G>A (p.Val138Met)	GPR158, GPR158-AS1 (V138M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3101567	NM_020752.3(GPR158):c.380A>T (p.Asp127Val)	GPR158, GPR158-AS1 (D127V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3101566	NM_020752.3(GPR158):c.3503G>A (p.Arg1168Gln)	GPR158 (R1168Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101565	NM_020752.3(GPR158):c.3455G>A (p.Arg1152His)	GPR158 (R1152H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101564	NM_020752.3(GPR158):c.3322C>A (p.Arg1108Ser)	GPR158 (R1108S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101563	NM_020752.3(GPR158):c.2912A>G (p.Gln971Arg)	GPR158 (Q971R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101561	NM_020752.3(GPR158):c.269A>C (p.Asp90Ala)	GPR158, GPR158-AS1 (D90A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3101560	NM_020752.3(GPR158):c.2075C>T (p.Ser692Phe)	GPR158 (S692F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101559	NM_020752.3(GPR158):c.2024G>A (p.Arg675Gln)	GPR158 (R675Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101558	NM_020752.3(GPR158):c.1972A>C (p.Thr658Pro)	GPR158 (T658P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101557	NM_020752.3(GPR158):c.1778G>T (p.Gly593Val)	GPR158 (G593V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101556	NM_020752.3(GPR158):c.1570G>A (p.Gly524Arg)	GPR158 (G524R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101555	NM_020752.3(GPR158):c.146C>T (p.Pro49Leu)	GPR158, GPR158-AS1 (P49L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101554	NM_020752.3(GPR158):c.1343G>A (p.Arg448Gln)	GPR158 (R448Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101553	NM_020752.3(GPR158):c.1220C>G (p.Pro407Arg)	GPR158 (P407R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101552	NM_020752.3(GPR158):c.1067C>A (p.Ala356Glu)	GPR158 (A356E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063151	GRCh37/hg19 10p12.1-11.23(chr10:25646101-30715668)x1	ABI1, ACBD5 +20 more	Copy number loss	not specified	GPathogenic
Select item 3063147	GRCh37/hg19 10p12.1(chr10:25747082-26352575)x3	GPR158, MYO3A	Copy number gain	not specified	GUncertain significance
Select item 2684600	GRCh37/hg19 10p12.2-12.1(chr10:24560328-25536166)x3	ARHGAP21, ENKUR +4 more	Copy number gain	not provided	GUncertain significance
Select item 2640360	NM_020752.3(GPR158):c.849T>C (p.Val283=)	GPR158, GPR158-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2623845	NM_020752.3(GPR158):c.3408A>C (p.Gln1136His)	GPR158 (Q1136H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616115	NM_020752.3(GPR158):c.484T>C (p.Trp162Arg)	GPR158, GPR158-AS1 (W162R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2599846	NM_020752.3(GPR158):c.2558C>T (p.Ser853Leu)	GPR158 (S853L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	AGAP5, CRTAC1 +682 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574686	GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	ABRAXAS2, CHCHD1 +673 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 2552348	NM_020752.3(GPR158):c.1627G>A (p.Gly543Ser)	GPR158 (G543S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542942	NM_020752.3(GPR158):c.2783G>A (p.Arg928His)	GPR158 (R928H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527345	NM_020752.3(GPR158):c.1712A>G (p.Asn571Ser)	GPR158 (N571S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518643	NM_020752.3(GPR158):c.287G>A (p.Arg96Gln)	GPR158, GPR158-AS1 (R96Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2515781	NM_020752.3(GPR158):c.1679G>A (p.Gly560Asp)	GPR158 (G560D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494122	NM_020752.3(GPR158):c.385C>A (p.Leu129Met)	GPR158, GPR158-AS1 (L129M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2492431	NM_020752.3(GPR158):c.3386C>T (p.Thr1129Ile)	GPR158 (T1129I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491035	NM_020752.3(GPR158):c.1724T>C (p.Ile575Thr)	GPR158 (I575T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460042	NM_020752.3(GPR158):c.3103G>A (p.Glu1035Lys)	GPR158 (E1035K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457857	NM_020752.3(GPR158):c.2299C>T (p.Arg767Trp)	GPR158 (R767W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454838	NM_020752.3(GPR158):c.3458G>A (p.Gly1153Asp)	GPR158 (G1153D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412322	NM_020752.3(GPR158):c.3410T>C (p.Ile1137Thr)	GPR158 (I1137T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402791	NM_020752.3(GPR158):c.1976T>C (p.Ile659Thr)	GPR158 (I659T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398013	NM_020752.3(GPR158):c.1036G>A (p.Val346Ile)	GPR158 (V346I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395119	NM_020752.3(GPR158):c.341C>T (p.Ala114Val)	GPR158, GPR158-AS1 (A114V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2387143	NM_020752.3(GPR158):c.962A>G (p.Asp321Gly)	GPR158 (D321G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380794	NM_020752.3(GPR158):c.1342C>T (p.Arg448Trp)	GPR158 (R448W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354969	NM_020752.3(GPR158):c.566A>T (p.Gln189Leu)	GPR158, GPR158-AS1 (Q189L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2330434	NM_020752.3(GPR158):c.328G>A (p.Gly110Arg)	GPR158, GPR158-AS1 (G110R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2314963	NM_020752.3(GPR158):c.2795A>G (p.Gln932Arg)	GPR158 (Q932R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2309278	NM_020752.3(GPR158):c.1510C>T (p.His504Tyr)	GPR158 (H504Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298782	NM_020752.3(GPR158):c.556C>G (p.Pro186Ala)	GPR158, GPR158-AS1 (P186A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2292369	NM_020752.3(GPR158):c.3239C>T (p.Ser1080Phe)	GPR158 (S1080F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290140	NM_020752.3(GPR158):c.2483C>G (p.Thr828Arg)	GPR158 (T828R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285005	NM_020752.3(GPR158):c.2489A>C (p.Glu830Ala)	GPR158 (E830A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281671	NM_020752.3(GPR158):c.3577T>A (p.Ser1193Thr)	GPR158 (S1193T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276088	NM_020752.3(GPR158):c.410A>G (p.Asn137Ser)	GPR158, GPR158-AS1 (N137S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2267021	NM_020752.3(GPR158):c.712G>A (p.Gly238Ser)	GPR158, GPR158-AS1 (G238S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2261571	NM_020752.3(GPR158):c.2716A>G (p.Ile906Val)	GPR158 (I906V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258914	NM_020752.3(GPR158):c.1940A>G (p.Tyr647Cys)	GPR158 (Y647C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255893	NM_020752.3(GPR158):c.116C>T (p.Thr39Ile)	GPR158, GPR158-AS1 (T39I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255240	NM_020752.3(GPR158):c.2429G>A (p.Arg810Gln)	GPR158 (R810Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245860	NM_020752.3(GPR158):c.860C>T (p.Ser287Phe)	GPR158 (S287F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232689	NM_020752.3(GPR158):c.1699C>T (p.His567Tyr)	GPR158 (H567Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226024	NM_020752.3(GPR158):c.2782C>T (p.Arg928Cys)	GPR158 (R928C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219199	NM_020752.3(GPR158):c.584C>T (p.Thr195Met)	GPR158, GPR158-AS1 (T195M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2209845	NM_020752.3(GPR158):c.170C>T (p.Ser57Phe)	GPR158, GPR158-AS1 (S57F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209776	NM_020752.3(GPR158):c.3538G>C (p.Ala1180Pro)	GPR158 (A1180P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207617	NM_020752.3(GPR158):c.1480A>G (p.Thr494Ala)	GPR158 (T494A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1527577	GRCh37/hg19 10p15.1-11.21(chr10:6273934-34732521)	ABI1, ACBD5 +111 more	Copy number gain	not specified	GPathogenic
Select item 1339781	GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4	ARL5B, LARP4B +180 more	Copy number gain	Mosaic supernumerary isodicentric chromosome 10	Gnot provided
Select item 1294578	NM_020752.3(GPR158):c.1274C>G (p.Ala425Gly)	GPR158 (A425G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 685790	GRCh37/hg19 10p12.1(chr10:25573964-25798996)x1	GPR158	Copy number loss	not provided	GUncertain significance
Select item 443842	GRCh37/hg19 10p12.1(chr10:24628319-26747630)x1	APBB1IP, ARHGAP21 +7 more	Copy number loss	See cases	GUncertain significance
Select item 443260	GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3	ABI1, ACBD5 +205 more	Copy number gain	See cases	GPathogenic
Select item 441987	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	INA, INPP5A +721 more	Copy number gain	See cases	GPathogenic
Select item 441986	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	A1CF, ABCC2 +721 more	Copy number gain	See cases	GPathogenic
Select item 393995	GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	A1CF, ABCC2 +722 more	Copy number gain	See cases	GPathogenic
Select item 152998	GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	ABI1, ACBD5 +1221 more	Copy number gain	See cases	GBenign
Select item 150600	GRCh38/hg38 10p12.31-11.22(chr10:19088161-32732293)x3	ABI1, ACBD5 +376 more	Copy number gain	See cases	GLikely pathogenic
Select item 149407	GRCh38/hg38 10p15.3-12.1(chr10:90205-26339978)x3	ACBD7, ACBD7-DCLRE1CP1 +837 more	Copy number gain	See cases	GPathogenic
Select item 144415	GRCh38/hg38 10p12.2-12.1(chr10:24111341-25350640)x1	GPR158-AS1, KIAA1217 +35 more	Copy number loss	See cases	GPathogenic
Select item 59666	GRCh38/hg38 10p12.1(chr10:25484473-26963308)x3	ABI1, ANKRD26 +38 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 91