ClinVar for Gene (Select 10260) - ClinVar

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Links from Gene

Items: 70

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3271567	NM_001320835.1(DENND4A):c.1786G>C (p.Ala596Pro)	DENND4A (A596P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271566	NM_001320835.1(DENND4A):c.2987G>A (p.Cys996Tyr)	DENND4A (C995Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271565	NM_001320835.1(DENND4A):c.238G>A (p.Gly80Arg)	DENND4A (G80R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271564	NM_001320835.1(DENND4A):c.4426G>A (p.Ala1476Thr)	DENND4A (A1432T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3271563	NM_001320835.1(DENND4A):c.4160T>C (p.Met1387Thr)	DENND4A (M1387T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081597	NM_001320835.1(DENND4A):c.5684T>C (p.Val1895Ala)	DENND4A (V1851A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081596	NM_001320835.1(DENND4A):c.5495A>G (p.Asn1832Ser)	DENND4A (N1788S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081593	NM_001320835.1(DENND4A):c.4166C>A (p.Thr1389Asn)	DENND4A (T1345N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081592	NM_001320835.1(DENND4A):c.3418A>G (p.Lys1140Glu)	DENND4A (K1139E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081591	NM_001320835.1(DENND4A):c.3388C>T (p.Pro1130Ser)	DENND4A (P1086S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3081590	NM_001320835.1(DENND4A):c.3070G>A (p.Gly1024Arg)	DENND4A (G1023R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081587	NM_001320835.1(DENND4A):c.2657G>A (p.Arg886Lys)	DENND4A (R886K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081586	NM_001320835.1(DENND4A):c.13A>G (p.Lys5Glu)	DENND4A (K5E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3065495	NM_001320835.1(DENND4A):c.2088C>G (p.Ser696Arg)	DENND4A (S696R)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2617548	NM_001320835.1(DENND4A):c.2983G>A (p.Asp995Asn)	DENND4A (D994N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617046	NM_001320835.1(DENND4A):c.5008C>T (p.His1670Tyr)	DENND4A (H1626Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615447	NM_001320835.1(DENND4A):c.4888A>G (p.Arg1630Gly)	DENND4A (R1586G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610395	NM_001320835.1(DENND4A):c.4265A>T (p.His1422Leu)	DENND4A (H1421L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604906	NM_001320835.1(DENND4A):c.2386G>A (p.Val796Met)	DENND4A (V796M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556795	NM_001320835.1(DENND4A):c.3218A>T (p.Asn1073Ile)	DENND4A (N1073I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555948	NM_001320835.1(DENND4A):c.3281A>C (p.Glu1094Ala)	DENND4A (E1094A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550057	NM_001320835.1(DENND4A):c.3820C>T (p.Arg1274Trp)	DENND4A (R1273W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546063	NM_001320835.1(DENND4A):c.1117C>T (p.His373Tyr)	DENND4A (H373Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544920	NM_001320835.1(DENND4A):c.4138A>G (p.Lys1380Glu)	DENND4A (K1379E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537708	NM_001320835.1(DENND4A):c.2491C>G (p.Arg831Gly)	DENND4A (R831G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529227	NM_001320835.1(DENND4A):c.2531A>G (p.Asn844Ser)	DENND4A (N844S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525662	NM_001320835.1(DENND4A):c.4427C>G (p.Ala1476Gly)	DENND4A (A1432G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518946	NM_001320835.1(DENND4A):c.2296C>T (p.Arg766Cys)	DENND4A (R766C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493769	NM_001320835.1(DENND4A):c.2962G>A (p.Glu988Lys)	DENND4A (E944K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482331	NM_001320835.1(DENND4A):c.1375G>A (p.Val459Ile)	DENND4A (V459I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473398	NM_001320835.1(DENND4A):c.3025G>A (p.Val1009Ile)	DENND4A (V1008I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471848	NM_001320835.1(DENND4A):c.4643A>G (p.Tyr1548Cys)	DENND4A (Y1504C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465730	NM_001320835.1(DENND4A):c.4459A>G (p.Met1487Val)	DENND4A (M1486V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460688	NM_001320835.1(DENND4A):c.4187G>T (p.Ser1396Ile)	DENND4A (S1395I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407177	NM_001320835.1(DENND4A):c.2821A>G (p.Arg941Gly)	DENND4A (R941G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404080	NM_001320835.1(DENND4A):c.1982G>A (p.Arg661Gln)	DENND4A (R661Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401227	NM_001320835.1(DENND4A):c.1640A>G (p.Tyr547Cys)	DENND4A (Y547C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377629	NM_001320835.1(DENND4A):c.380G>A (p.Arg127His)	DENND4A (R127H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368902	NM_001320835.1(DENND4A):c.3574C>T (p.Arg1192Cys)	DENND4A (R1192C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359438	NM_001320835.1(DENND4A):c.2060A>G (p.Asn687Ser)	DENND4A (N687S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357396	NM_001320835.1(DENND4A):c.136A>G (p.Thr46Ala)	DENND4A (T46A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349963	NM_001320835.1(DENND4A):c.3035C>T (p.Thr1012Ile)	DENND4A (T1011I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349575	NM_001320835.1(DENND4A):c.4439A>G (p.Asn1480Ser)	DENND4A (N1480S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349121	NM_001320835.1(DENND4A):c.4288T>A (p.Ser1430Thr)	DENND4A (S1386T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347982	NM_001320835.1(DENND4A):c.1827C>G (p.Asp609Glu)	DENND4A (D609E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330504	NM_001320835.1(DENND4A):c.971C>G (p.Ala324Gly)	DENND4A (A324G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327576	NM_001320835.1(DENND4A):c.4855G>C (p.Ala1619Pro)	DENND4A (A1619P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321149	NM_001320835.1(DENND4A):c.2071C>A (p.Pro691Thr)	DENND4A (P691T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319950	NM_001320835.1(DENND4A):c.5470A>G (p.Met1824Val)	DENND4A (M1780V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318382	NM_001320835.1(DENND4A):c.4375C>G (p.Leu1459Val)	DENND4A (L1458V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316069	NM_001320835.1(DENND4A):c.3182A>G (p.Asn1061Ser)	DENND4A (N1017S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314054	NM_001320835.1(DENND4A):c.1680G>T (p.Leu560Phe)	DENND4A (L560F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289672	NM_001320835.1(DENND4A):c.765T>G (p.Phe255Leu)	DENND4A (F255L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287783	NM_001320835.1(DENND4A):c.538G>A (p.Asp180Asn)	DENND4A (D180N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269253	NM_001320835.1(DENND4A):c.1145T>C (p.Val382Ala)	DENND4A (V382A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269229	NM_001320835.1(DENND4A):c.364A>C (p.Ser122Arg)	DENND4A (S122R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245949	NM_001320835.1(DENND4A):c.4084G>A (p.Val1362Ile)	DENND4A (V1361I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244636	NM_001320835.1(DENND4A):c.2474A>G (p.Gln825Arg)	DENND4A (Q825R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222211	NM_001320835.1(DENND4A):c.5647A>G (p.Ser1883Gly)	DENND4A (S1883G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1024934	NC_000015.9:g.(?_32964879)_(91358519_?)dup	CGNL1, MAPDA +472 more	Duplication	Familial colorectal cancer +1 more	GUncertain significance
Select item 560063	Single allele	ANKDD1A, APH1B +40 more	Deletion	Nemaline myopathy 6	GLikely pathogenic
Select item 560049	Single allele	PDIA3, PEAK1 +521 more	Duplication	not provided	GPathogenic
Select item 442893	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3	AAGAB, ABHD17C +559 more	Copy number gain	See cases	GPathogenic
Select item 442892	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)	NOX5, NPAP1 +559 more	Copy number gain	See cases	GPathogenic
Select item 395145	GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4	CHRFAM7A, CHRM5 +566 more	Copy number gain	See cases	GPathogenic
Select item 394887	GRCh37/hg19 15q15.1-26.3(chr15:41745084-102354798)x4	ALDH1A2, ALDH1A3 +444 more	Copy number gain	See cases	GPathogenic
Select item 369835	GRCh37/hg19 15q22.1-26.3(chr15:59297293-102480888)x3	WHAMM, CCNB2 +308 more	Copy number gain	not provided	GLikely pathogenic
Select item 253516	GRCh37/hg19 15q22.31-26.3(chr15:64637227-102509910)x3	AAGAB, ABHD17C +278 more	Copy number gain	See cases	GPathogenic
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057927, LOC130057928 +1764 more	Copy number gain	See cases	GPathogenic
Select item 58573	GRCh38/hg38 15q22.31(chr15:64448836-65975439)x3	ANKDD1A, CILP +97 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 70