ClinVar for Gene (Select 90627) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3323098	NM_178006.4(STARD13):c.1069A>G (p.Asn357Asp)	STARD13 (N342D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323097	NM_178006.4(STARD13):c.2495T>A (p.Val832Asp)	STARD13 (V832D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323096	NM_178006.4(STARD13):c.2386G>A (p.Val796Ile)	STARD13 (V678I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323095	NM_178006.4(STARD13):c.1875G>A (p.Thr625=)	STARD13	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3323094	NM_178006.4(STARD13):c.1561C>T (p.Pro521Ser)	STARD13 (P506S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323093	NM_178006.4(STARD13):c.2789C>T (p.Thr930Met)	STARD13 (T812M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323092	NM_178006.4(STARD13):c.179C>T (p.Ala60Val)	STARD13 (A45V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3170952	NM_178006.4(STARD13):c.3019C>T (p.His1007Tyr)	STARD13 (H1007Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170951	NM_178006.4(STARD13):c.2935G>A (p.Glu979Lys)	STARD13 (E979K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170950	NM_178006.4(STARD13):c.2921G>A (p.Arg974His)	STARD13 (R856H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170949	NM_178006.4(STARD13):c.2489C>T (p.Pro830Leu)	STARD13 (P712L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170947	NM_178006.4(STARD13):c.2383G>C (p.Asp795His)	STARD13 (D677H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170946	NM_178006.4(STARD13):c.2293G>C (p.Glu765Gln)	STARD13 (E730Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170945	NM_178006.4(STARD13):c.1532T>C (p.Leu511Pro)	STARD13 (L476P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170944	NM_178006.4(STARD13):c.1333C>T (p.Arg445Trp)	STARD13 (R410W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170943	NM_178006.4(STARD13):c.1313T>C (p.Val438Ala)	STARD13 (V320A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170942	NM_178006.4(STARD13):c.106C>T (p.Arg36Cys)	STARD13 (R36C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3148850	GRCh37/hg19 13q11-13.3(chr13:19436287-36278224)x3	CDX2, AMER2 +82 more	Copy number gain	not provided	GUncertain significance
Select item 2643736	NM_178006.4(STARD13):c.750G>A (p.Lys250=)	STARD13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643735	NM_178006.4(STARD13):c.1344G>A (p.Ala448=)	STARD13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2623629	NM_178006.4(STARD13):c.1580C>T (p.Pro527Leu)	STARD13 (P512L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590660	NM_178006.4(STARD13):c.3017C>A (p.Pro1006His)	STARD13 (P991H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589395	NM_178006.4(STARD13):c.2968C>G (p.Leu990Val)	STARD13 (L955V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561386	NM_178006.4(STARD13):c.1577T>C (p.Phe526Ser)	STARD13 (F408S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554534	NM_178006.4(STARD13):c.989G>A (p.Ser330Asn)	STARD13 (S295N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554360	NM_178006.4(STARD13):c.2975G>A (p.Arg992Lys)	STARD13 (R874K +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2553059	NM_178006.4(STARD13):c.869T>C (p.Met290Thr)	STARD13 (M290T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548567	NM_178006.4(STARD13):c.3120G>C (p.Gln1040His)	STARD13 (Q1005H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544854	NM_178006.4(STARD13):c.3215T>C (p.Ile1072Thr)	STARD13 (I1037T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537560	NM_178006.4(STARD13):c.1004C>T (p.Pro335Leu)	STARD13 (P217L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536341	NM_178006.4(STARD13):c.1675A>G (p.Asn559Asp)	STARD13 (N441D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525703	NM_178006.4(STARD13):c.1594A>G (p.Ile532Val)	STARD13 (I517V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525519	NM_178006.4(STARD13):c.3274G>A (p.Ala1092Thr)	STARD13 (A1084T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525472	NM_178006.4(STARD13):c.1007C>T (p.Ser336Leu)	STARD13 (S301L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522514	NM_178006.4(STARD13):c.2195C>T (p.Ala732Val)	STARD13 (A717V +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2493675	NM_178006.4(STARD13):c.71A>G (p.Gln24Arg)	STARD13 (Q24R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492536	NM_178006.4(STARD13):c.2219G>A (p.Arg740Gln)	STARD13 (R725Q +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2491829	NM_178006.4(STARD13):c.400G>A (p.Asp134Asn)	STARD13 (D99N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480499	NM_178006.4(STARD13):c.1146C>A (p.Ser382Arg)	STARD13 (S367R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476772	NM_178006.4(STARD13):c.1930C>T (p.Pro644Ser)	STARD13 (P636S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470541	NM_178006.4(STARD13):c.1624T>G (p.Ser542Ala)	STARD13 (S507A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467661	NM_178006.4(STARD13):c.3158A>G (p.Gln1053Arg)	STARD13 (Q1018R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459782	NM_178006.4(STARD13):c.784C>T (p.Arg262Cys)	STARD13 (R254C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412356	NM_178006.4(STARD13):c.2095C>T (p.Arg699Cys)	STARD13 (R581C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411342	NM_178006.4(STARD13):c.1633C>T (p.Arg545Trp)	STARD13 (R427W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407427	NM_178006.4(STARD13):c.2423T>C (p.Met808Thr)	STARD13 (M800T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396697	NM_178006.4(STARD13):c.77T>C (p.Met26Thr)	STARD13 (M26T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396280	NM_178006.4(STARD13):c.482C>T (p.Thr161Met)	STARD13 (T146M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395410	NM_178006.4(STARD13):c.1867C>T (p.Arg623Cys)	STARD13 (R588C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393750	NM_178006.4(STARD13):c.1940T>C (p.Met647Thr)	STARD13 (M529T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391287	NM_178006.4(STARD13):c.1751G>A (p.Arg584Gln)	STARD13 (R569Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381255	NM_178006.4(STARD13):c.659C>T (p.Pro220Leu)	STARD13 (P185L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373922	NM_178006.4(STARD13):c.1012C>A (p.His338Asn)	STARD13 (H323N +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2370320	NM_178006.4(STARD13):c.1789C>T (p.Arg597Trp)	STARD13 (R479W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369997	NM_178006.4(STARD13):c.622A>T (p.Ser208Cys)	STARD13 (S173C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366511	NM_178006.4(STARD13):c.3017C>T (p.Pro1006Leu)	STARD13 (P1006L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363589	NM_178006.4(STARD13):c.1342G>A (p.Ala448Thr)	STARD13 (A433T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355293	NM_178006.4(STARD13):c.1846C>T (p.Leu616Phe)	STARD13 (L601F +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352443	NM_178006.4(STARD13):c.56T>C (p.Met19Thr)	STARD13 (M19T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338921	NM_178006.4(STARD13):c.2762C>T (p.Ala921Val)	STARD13 (A886V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338767	NM_178006.4(STARD13):c.1844T>C (p.Leu615Pro)	STARD13 (L497P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338394	NM_178006.4(STARD13):c.1574C>T (p.Thr525Ile)	STARD13 (T510I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330316	NM_178006.4(STARD13):c.1757G>A (p.Arg586Gln)	STARD13 (R586Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329133	NM_178006.4(STARD13):c.1405G>T (p.Ala469Ser)	STARD13 (A351S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312403	NM_178006.4(STARD13):c.827A>G (p.Lys276Arg)	STARD13 (K241R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300285	NM_178006.4(STARD13):c.734A>G (p.His245Arg)	STARD13 (H245R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297494	NM_178006.4(STARD13):c.1793C>G (p.Pro598Arg)	STARD13 (P563R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297277	NM_178006.4(STARD13):c.539C>T (p.Thr180Met)	STARD13 (T180M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293674	NM_178006.4(STARD13):c.2419C>T (p.Pro807Ser)	STARD13 (P792S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290878	NM_178006.4(STARD13):c.1985G>C (p.Gly662Ala)	STARD13 (G544A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284127	NM_178006.4(STARD13):c.3032A>C (p.Asp1011Ala)	STARD13 (D996A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283081	NM_178006.4(STARD13):c.1874C>T (p.Thr625Met)	STARD13 (T507M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277330	NM_178006.4(STARD13):c.47T>A (p.Leu16Gln)	STARD13 (L16Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2268721	NM_178006.4(STARD13):c.408A>T (p.Glu136Asp)	STARD13 (E121D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259844	NM_178006.4(STARD13):c.602A>G (p.Glu201Gly)	STARD13 (E166G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253335	NM_178006.4(STARD13):c.469G>T (p.Asp157Tyr)	STARD13 (D142Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232690	NM_178006.4(STARD13):c.1759T>C (p.Trp587Arg)	STARD13 (W469R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211146	NM_178006.4(STARD13):c.142C>A (p.His48Asn)	STARD13 (H48N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208458	NM_178006.4(STARD13):c.1076G>A (p.Arg359His)	STARD13 (R241H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204357	NM_178006.4(STARD13):c.1634G>A (p.Arg545Gln)	STARD13 (R537Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1810291	GRCh37/hg19 13q12.3-13.3(chr13:31841196-36667007)x3	B3GLCT, BRCA2 +12 more	Copy number gain	not provided	Gnot provided
Select item 1808763	GRCh37/hg19 13q13.1-13.2(chr13:33504270-34507428)x4	KL, RFC3 +1 more	Copy number gain	not provided	GUncertain significance
Select item 1710518	GRCh37/hg19 13q11-34(chr13:19253848-115108937)x3	B3GLCT, HS6ST3 +332 more	Copy number gain	not provided	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 1527762	GRCh37/hg19 13q13.1-21.31(chr13:32946120-62698217)	AKAP11, ALG11 +127 more	Copy number loss	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 1341081	GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	ABCC4, ABHD13 +332 more	Copy number gain	not provided	GPathogenic
Select item 1341070	GRCh37/hg19 13q13.1-13.2(chr13:33890716-34512958)x3	RFC3, STARD13	Copy number gain	not provided	GUncertain significance
Select item 1321996	GRCh37/hg19 13p13-q34(chr13:1-115169878)x3	DACH1, IRS2 +332 more	Copy number gain	See cases	GPathogenic
Select item 1180526	GRCh37/hg19 13q12.3-13.2(chr13:28925153-34061696)x1	ALOX5AP, B3GLCT +22 more	Copy number loss	not provided	GPathogenic
Select item 1048617	GRCh37/hg19 13q11-34(chr13:19053605-115108528)x3	CENPJ, CHAMP1 +332 more	Copy number gain	See cases	GPathogenic
Select item 791588	NM_178006.4(STARD13):c.3174G>A (p.Pro1058=)	STARD13	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 786239	NM_178006.4(STARD13):c.2790G>A (p.Thr930=)	STARD13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 785444	NM_178006.4(STARD13):c.3022C>T (p.Pro1008Ser)	STARD13 (P1000S +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 776795	NM_178006.4(STARD13):c.495A>T (p.Arg165=)	STARD13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 776794	NM_178006.4(STARD13):c.1275T>C (p.Asn425=)	STARD13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775342	NM_178006.4(STARD13):c.468G>A (p.Val156=)	STARD13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775341	NM_178006.4(STARD13):c.1116G>T (p.Gly372=)	STARD13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 742749	NM_178006.4(STARD13):c.1113G>A (p.Ala371=)	STARD13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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