List of variants in gene SETX reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 51

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HGVS	dbSNP	gnomAD frequency
NM_015046.7(SETX):c.7724C>T (p.Pro2575Leu)	rs34000644	0.00304
NM_015046.7(SETX):c.3010A>G (p.Asn1004Asp)	rs77984885	0.00075
NM_015046.7(SETX):c.2479A>G (p.Lys827Glu)	rs150532677	0.00058
NM_015046.7(SETX):c.654G>C (p.Lys218Asn)	rs117861188	0.00039
NM_015046.7(SETX):c.7738G>A (p.Val2580Ile)	rs370366576	0.00013
NM_015046.7(SETX):c.2750T>C (p.Met917Thr)	rs376022544	0.00009
NM_015046.7(SETX):c.1690T>G (p.Leu564Val)	rs761877146	0.00006
NM_015046.7(SETX):c.3016G>A (p.Gly1006Arg)	rs141266068	0.00006
NM_015046.7(SETX):c.2862G>A (p.Thr954=)	rs149610510	0.00005
NM_015046.7(SETX):c.4225A>T (p.Asn1409Tyr)	rs373375060	0.00005
NM_015046.7(SETX):c.4865C>T (p.Pro1622Leu)	rs140781535	0.00005
NM_015046.7(SETX):c.3968G>A (p.Arg1323Gln)	rs369542231	0.00004
NM_015046.7(SETX):c.6910G>T (p.Asp2304Tyr)	rs774458684	0.00004
NM_015046.7(SETX):c.2755G>C (p.Val919Leu)	rs561190371	0.00003
NM_015046.7(SETX):c.3117A>G (p.Ile1039Met)	rs886063555	0.00003
NM_015046.7(SETX):c.503G>A (p.Arg168Gln)	rs772017103	0.00003
NM_015046.7(SETX):c.806C>T (p.Ser269Leu)	rs757988188	0.00003
NM_015046.7(SETX):c.2395C>T (p.His799Tyr)	rs200459144	0.00002
NM_015046.7(SETX):c.2842C>A (p.Pro948Thr)	rs778882347	0.00002
NM_015046.7(SETX):c.2921T>C (p.Ile974Thr)	rs765768857	0.00002
NM_015046.7(SETX):c.5552G>A (p.Arg1851His)	rs137978070	0.00002
NM_015046.7(SETX):c.7163C>T (p.Thr2388Met)	rs765418950	0.00002
NM_015046.7(SETX):c.1505G>A (p.Arg502Gln)	rs750044197	0.00001
NM_015046.7(SETX):c.172C>T (p.His58Tyr)	rs757760067	0.00001
NM_015046.7(SETX):c.2329A>G (p.Lys777Glu)	rs771595581	0.00001
NM_015046.7(SETX):c.3028C>T (p.Arg1010Cys)	rs766799023	0.00001
NM_015046.7(SETX):c.3221A>G (p.Glu1074Gly)	rs752140967	0.00001
NM_015046.7(SETX):c.383G>A (p.Arg128His)	rs749887957	0.00001
NM_015046.7(SETX):c.4045C>G (p.Gln1349Glu)	rs146407699	0.00001
NM_015046.7(SETX):c.4120A>G (p.Lys1374Glu)	rs756823072	0.00001
NM_015046.7(SETX):c.5501A>G (p.His1834Arg)	rs770822383	0.00001
NM_015046.7(SETX):c.5804A>G (p.Asn1935Ser)	rs762791927	0.00001
NM_015046.7(SETX):c.6689T>C (p.Met2230Thr)	rs753109637	0.00001
NM_015046.7(SETX):c.7103C>G (p.Pro2368Arg)	rs1420833435	0.00001
NM_015046.7(SETX):c.7139G>A (p.Arg2380Gln)	rs145397619	0.00001
NM_015046.7(SETX):c.1097A>G (p.Lys366Arg)	rs1554822056
NM_015046.7(SETX):c.12TTG[1] (p.Cys5del)	rs774123592
NM_015046.7(SETX):c.1658C>T (p.Ser553Phe)	rs1589747116
NM_015046.7(SETX):c.1729A>T (p.Thr577Ser)	rs1205251772
NM_015046.7(SETX):c.1948A>G (p.Met650Val)
NM_015046.7(SETX):c.2749A>G (p.Met917Val)	rs761943404
NM_015046.7(SETX):c.3057TGA[4] (p.Asp1023_Asp1024del)	rs572772837
NM_015046.7(SETX):c.3456T>G (p.Phe1152Leu)	rs1554820870
NM_015046.7(SETX):c.4217C>G (p.Ala1406Gly)	rs113856732
NM_015046.7(SETX):c.5274+5G>A	rs192596579
NM_015046.7(SETX):c.5375-9G>A
NM_015046.7(SETX):c.6112T>C (p.Cys2038Arg)	rs1554809388
NM_015046.7(SETX):c.6691G>T (p.Ala2231Ser)
NM_015046.7(SETX):c.7157T>C (p.Ile2386Thr)	rs201887051
NM_015046.7(SETX):c.7708CCT[1] (p.Pro2571del)	rs770590408
NM_015046.7(SETX):c.7943C>T (p.Ser2648Phe)	rs1014113627

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