ClinVar for Gene (Select 283316) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140588	NM_001080454.2(ACSM4):c.1403T>A (p.Val468Asp)	ACSM4, CD163L1 +1 more (V468D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140330	NM_174941.6(CD163L1):c.955T>A (p.Ser319Thr)	CD163L1 (S329T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140329	NM_174941.6(CD163L1):c.822A>T (p.Arg274Ser)	CD163L1 (R274S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140328	NM_174941.6(CD163L1):c.818G>A (p.Gly273Glu)	CD163L1 (G273E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140327	NM_174941.6(CD163L1):c.814A>G (p.Met272Val)	CD163L1 (M282V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140326	NM_174941.6(CD163L1):c.643C>A (p.Arg215Ser)	CD163L1 (R215S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140325	NM_174941.6(CD163L1):c.4315G>A (p.Asp1439Asn)	CD163L1 (D1439N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140324	NM_174941.6(CD163L1):c.4060A>G (p.Asn1354Asp)	CD163L1, LOC126861436 (N1354D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140323	NM_174941.6(CD163L1):c.4011C>G (p.His1337Gln)	CD163L1, LOC126861436 (H1337Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140322	NM_174941.6(CD163L1):c.3979G>A (p.Ala1327Thr)	CD163L1, LOC126861436 (A1327T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140321	NM_174941.6(CD163L1):c.3940C>T (p.Arg1314Trp)	CD163L1, LOC126861436 (R1324W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140320	NM_174941.6(CD163L1):c.3160G>C (p.Asp1054His)	CD163L1 (D1064H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140319	NM_174941.6(CD163L1):c.3034G>A (p.Ala1012Thr)	CD163L1 (A1022T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140318	NM_174941.6(CD163L1):c.2882G>C (p.Arg961Pro)	CD163L1 (R961P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140317	NM_174941.6(CD163L1):c.2434C>T (p.His812Tyr)	CD163L1 (H812Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140316	NM_174941.6(CD163L1):c.2333C>T (p.Ala778Val)	CD163L1 (A778V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140315	NM_174941.6(CD163L1):c.2177T>C (p.Val726Ala)	CD163L1 (V726A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140314	NM_174941.6(CD163L1):c.1735G>A (p.Ala579Thr)	CD163L1 (A579T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140313	NM_174941.6(CD163L1):c.1379G>A (p.Arg460Gln)	CD163L1 (R460Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140312	NM_174941.6(CD163L1):c.1327T>A (p.Ser443Thr)	CD163L1 (S453T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063250	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835641)x3	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 3024838	NM_174941.6(CD163L1):c.4066T>C (p.Ser1356Pro)	CD163L1, LOC126861436 (S1356P +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3024755	NM_174941.6(CD163L1):c.1772G>T (p.Arg591Leu)	CD163L1 (R591L +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2671607	Single allele	FGD4, FGF23 +278 more	Duplication	not provided	GPathogenic
Select item 2642679	NM_174941.6(CD163L1):c.3163G>A (p.Gly1055Ser)	CD163L1 (G1055S +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2642678	NM_174941.6(CD163L1):c.3243G>A (p.Val1081=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642677	NM_174941.6(CD163L1):c.3261C>G (p.Val1087=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642676	NM_174941.6(CD163L1):c.3273T>C (p.Phe1091=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642675	NM_174941.6(CD163L1):c.3279G>A (p.Glu1093=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642674	NM_174941.6(CD163L1):c.3282G>A (p.Gly1094=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642673	NM_174941.6(CD163L1):c.3303T>C (p.Asp1101=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642672	NM_174941.6(CD163L1):c.3354C>G (p.Arg1118=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642671	NM_174941.6(CD163L1):c.3378G>A (p.Arg1126=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642670	NM_174941.6(CD163L1):c.3393A>C (p.Ala1131=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642669	NM_174941.6(CD163L1):c.3393A>G (p.Ala1131=)	CD163L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2624318	NM_174941.6(CD163L1):c.3524C>T (p.Ala1175Val)	CD163L1 (A1175V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614548	NM_174941.6(CD163L1):c.4252G>C (p.Glu1418Gln)	CD163L1 (E1418Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605051	NM_174941.6(CD163L1):c.3644C>T (p.Thr1215Met)	CD163L1 (T1215M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600229	NM_174941.6(CD163L1):c.3760G>A (p.Glu1254Lys)	CD163L1, LOC126861436 (E1264K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597605	NM_174941.6(CD163L1):c.3242T>A (p.Val1081Glu)	CD163L1 (V1091E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595920	NM_174941.6(CD163L1):c.485A>G (p.Asn162Ser)	CD163L1 (N162S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2569915	NM_174941.6(CD163L1):c.1696G>A (p.Val566Ile)	CD163L1 (V576I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2568287	NM_174941.6(CD163L1):c.2861A>G (p.Tyr954Cys)	CD163L1 (Y954C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558655	NM_174941.6(CD163L1):c.3526A>G (p.Ile1176Val)	CD163L1 (I1176V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543561	NM_174941.6(CD163L1):c.2449C>T (p.Arg817Cys)	CD163L1 (R817C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515857	NM_174941.6(CD163L1):c.2095T>A (p.Cys699Ser)	CD163L1 (C699S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494087	NM_174941.6(CD163L1):c.323G>A (p.Gly108Glu)	CD163L1 (G108E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487944	NM_174941.6(CD163L1):c.3137C>T (p.Ala1046Val)	CD163L1 (A1046V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478569	NM_174941.6(CD163L1):c.1955G>A (p.Cys652Tyr)	CD163L1 (C662Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476995	NM_174941.6(CD163L1):c.2083G>A (p.Gly695Arg)	CD163L1 (G705R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475889	NM_174941.6(CD163L1):c.2063T>C (p.Met688Thr)	CD163L1 (M688T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469014	NM_174941.6(CD163L1):c.1637T>C (p.Ile546Thr)	CD163L1 (I546T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468353	NM_174941.6(CD163L1):c.286G>A (p.Ala96Thr)	CD163L1 (A96T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2467885	NM_174941.6(CD163L1):c.2999C>G (p.Thr1000Arg)	CD163L1 (T1000R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464631	NM_174941.6(CD163L1):c.1612A>G (p.Ile538Val)	CD163L1 (I548V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2445417	GRCh37/hg19 12p13.33-11.1(chr12:176047-34179852)x4	AKAP3, ETFRF1 +278 more	Copy number gain	Pallister-Killian syndrome	GPathogenic
Select item 2423987	NC_000012.11:g.(?_4368352)_(9027607_?)dup	A2ML1, ACRBP +85 more	Duplication	Lymphoproliferative syndrome 2	GUncertain significance
Select item 2409250	NM_001080454.2(ACSM4):c.961C>A (p.Pro321Thr)	ACSM4, CD163L1 (P321T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402042	NM_174941.6(CD163L1):c.3353G>A (p.Arg1118His)	CD163L1 (R1118H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2400540	NM_174941.6(CD163L1):c.2879T>C (p.Val960Ala)	CD163L1 (V960A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379250	NM_174941.6(CD163L1):c.1676G>T (p.Gly559Val)	CD163L1 (G569V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377397	NM_174941.6(CD163L1):c.906G>C (p.Gln302His)	CD163L1 (Q312H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377287	NM_174941.6(CD163L1):c.2260A>G (p.Met754Val)	CD163L1 (M754V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369318	NM_174941.6(CD163L1):c.1258C>T (p.Arg420Cys)	CD163L1 (R420C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365662	NM_174941.6(CD163L1):c.3583G>A (p.Ala1195Thr)	CD163L1 (A1205T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358753	NM_174941.6(CD163L1):c.3131G>A (p.Arg1044His)	CD163L1 (R1044H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353953	NM_174941.6(CD163L1):c.3650T>G (p.Ile1217Ser)	CD163L1 (I1217S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352039	NM_001080454.2(ACSM4):c.1528C>T (p.Arg510Cys)	ACSM4, CD163L1 +1 more (R510C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349164	NM_174941.6(CD163L1):c.2183G>A (p.Cys728Tyr)	CD163L1 (C738Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348545	NM_174941.6(CD163L1):c.3657A>G (p.Ile1219Met)	CD163L1 (I1219M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344862	NM_174941.6(CD163L1):c.368C>G (p.Ala123Gly)	CD163L1 (A123G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339987	NM_174941.6(CD163L1):c.1043A>G (p.Asn348Ser)	CD163L1 (N348S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337284	NM_174941.6(CD163L1):c.394T>C (p.Trp132Arg)	CD163L1 (W132R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334483	NM_174941.6(CD163L1):c.1630T>C (p.Ser544Pro)	CD163L1 (S544P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330531	NM_174941.6(CD163L1):c.3790G>T (p.Ala1264Ser)	CD163L1, LOC126861436 (A1264S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322427	NM_174941.6(CD163L1):c.2950C>A (p.Leu984Ile)	CD163L1 (L994I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319720	NM_174941.6(CD163L1):c.4276T>C (p.Ser1426Pro)	CD163L1 (S1426P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317769	NM_174941.6(CD163L1):c.260A>G (p.Lys87Arg)	CD163L1 (K87R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312524	NM_174941.6(CD163L1):c.1048G>T (p.Asp350Tyr)	CD163L1 (D350Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308206	NM_174941.6(CD163L1):c.2170G>T (p.Ala724Ser)	CD163L1 (A724S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290694	NM_174941.6(CD163L1):c.3499G>A (p.Val1167Ile)	CD163L1 (V1167I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289171	NM_174941.6(CD163L1):c.485A>C (p.Asn162Thr)	CD163L1 (N172T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288022	NM_174941.6(CD163L1):c.1721C>T (p.Thr574Ile)	CD163L1 (T574I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2280578	NM_174941.6(CD163L1):c.3803G>A (p.Gly1268Asp)	CD163L1, LOC126861436 (G1278D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280149	NM_174941.6(CD163L1):c.641T>G (p.Leu214Trp)	CD163L1 (L214W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275866	NM_174941.6(CD163L1):c.1223A>G (p.Lys408Arg)	CD163L1 (K418R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268669	NM_001080454.2(ACSM4):c.1595T>C (p.Leu532Ser)	ACSM4, CD163L1 (L532S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260593	NM_174941.6(CD163L1):c.389G>A (p.Arg130Gln)	CD163L1 (R130Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242747	NM_174941.6(CD163L1):c.2450G>A (p.Arg817His)	CD163L1 (R827H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242130	NM_174941.6(CD163L1):c.3034G>T (p.Ala1012Ser)	CD163L1 (A1012S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2225043	NM_174941.6(CD163L1):c.3110G>A (p.Arg1037His)	CD163L1 (R1037H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217295	NM_174941.6(CD163L1):c.2473T>C (p.Ser825Pro)	CD163L1 (S835P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212334	NM_174941.6(CD163L1):c.2941A>G (p.Met981Val)	CD163L1 (M981V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2211725	NM_001080454.2(ACSM4):c.1705C>T (p.Arg569Cys)	ACSM4, CD163L1 (R569C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1807708	GRCh37/hg19 12p13.33-13.31(chr12:173787-8320544)x3	ACRBP, ACSM4 +105 more	Copy number gain	not provided	GPathogenic
Select item 1527672	GRCh37/hg19 12p13.33-q11(chr12:173786-37869301)	C3AR1, CACNA1C +278 more	Copy number gain	not specified	GPathogenic
Select item 1527671	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 1527669	GRCh37/hg19 12p13.33-12.1(chr12:173786-25286865)	A2ML1, ABCC9 +235 more	Copy number gain	not specified	GPathogenic
Select item 1473612	NC_000012.11:g.(?_6438478)_(8756953_?)dup	USP5, VAMP1 +64 more	Duplication	not provided	GUncertain significance
Select item 1409561	NC_000012.11:g.(?_6438478)_(8248686_?)dup	GDF3, GNB3 +57 more	Duplication	Temtamy syndrome	GUncertain significance

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