ClinVar Miner

List of variants in gene DST reported by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP gnomAD frequency
NM_001723.7(DST):c.6031G>C (p.Val2011Leu) rs6459166 0.42446
NM_001723.7(DST):c.4074G>A (p.Lys1358=) rs2230862 0.40815
NM_001374736.1(DST):c.2368T>C (p.Leu790=) rs2144407 0.14274
NM_001723.7(DST):c.98T>C (p.Leu33Ser) rs1024196 0.14270
NM_001723.7(DST):c.4980A>C (p.Val1660=) rs2230863 0.03282
NM_001723.7(DST):c.5055T>C (p.Asn1685=) rs2230864 0.03211
NM_001374736.1(DST):c.4930-367C>T rs150986597 0.02538
NM_001723.7(DST):c.7765A>G (p.Ile2589Val) rs150191284 0.02534
NM_001723.7(DST):c.6633A>G (p.Ala2211=) rs115542549 0.02533
NM_001374736.1(DST):c.4452T>C (p.Asn1484=) rs112640831 0.02508
NM_001374736.1(DST):c.4590T>G (p.Asn1530Lys) rs35014998 0.02397
NM_001723.7(DST):c.3346C>T (p.His1116Tyr) rs6909714 0.02098
NM_001723.7(DST):c.3809A>G (p.Lys1270Arg) rs35497571 0.02037
NM_001374736.1(DST):c.4930-864A>C rs17674547 0.01739
NM_001374736.1(DST):c.4062C>T (p.Val1354=) rs78600049 0.01311
NM_001374736.1(DST):c.3492C>T (p.Asn1164=) rs79026338 0.01176
NM_001723.7(DST):c.4289C>T (p.Ala1430Val) rs78701610 0.01093
NM_001723.7(DST):c.5485C>G (p.Gln1829Glu) rs79943354 0.01087
NM_001374736.1(DST):c.4831-3C>A rs115890942 0.01035
NM_001374736.1(DST):c.4200A>G (p.Lys1400=) rs35715547 0.00947
NM_001374736.1(DST):c.4930-300A>T rs75951731 0.00849
NM_001374736.1(DST):c.2520A>C (p.Ser840=) rs139336917 0.00635
NM_001723.7(DST):c.7491G>A (p.Lys2497=) rs145891100 0.00518
NM_001723.7(DST):c.3336G>C (p.Glu1112Asp) rs34767818 0.00349
NM_001723.7(DST):c.4400G>A (p.Arg1467His) rs147704763 0.00292
NM_001723.7(DST):c.4674C>T (p.Leu1558=) rs191617697 0.00285
NM_001723.7(DST):c.5909T>C (p.Phe1970Ser) rs141573097 0.00280
NM_001723.7(DST):c.5153A>C (p.Lys1718Thr) rs45487998 0.00245
NM_001374736.1(DST):c.2256A>T (p.Ser752=) rs113432929 0.00225
NM_001374736.1(DST):c.4906T>C (p.Leu1636=) rs147406105 0.00195
NM_001723.7(DST):c.25C>T (p.Arg9Cys) rs75671065 0.00193
NM_001374736.1(DST):c.4930-651G>A rs116219382 0.00155
NM_001374736.1(DST):c.2350C>G (p.Pro784Ala) rs151271595 0.00152
NM_001723.7(DST):c.4049C>T (p.Thr1350Met) rs45472691 0.00137
NM_001374736.1(DST):c.1779-395G>A rs143726337 0.00133
NM_001723.7(DST):c.6582A>C (p.Ala2194=) rs149007397 0.00115
NM_001374736.1(DST):c.2504G>A (p.Arg835His) rs41267671 0.00068
NM_001723.7(DST):c.3436A>G (p.Met1146Val) rs148413592 0.00066
NM_001723.7(DST):c.5930C>G (p.Thr1977Arg) rs148856756 0.00065
NM_001374736.1(DST):c.4930-430A>G rs140470023 0.00059
NM_001374736.1(DST):c.2042G>A (p.Arg681His) rs143101723 0.00058
NM_001723.7(DST):c.6868A>G (p.Arg2290Gly) rs112473525 0.00047
NM_001374736.1(DST):c.4638+7A>T rs185349093 0.00041
NM_001374736.1(DST):c.2125A>G (p.Met709Val) rs142650835 0.00039
NM_001374736.1(DST):c.4046C>T (p.Ala1349Val) rs150656535 0.00029
NM_001374736.1(DST):c.3964-11C>T rs371499560 0.00028
NM_001723.7(DST):c.7284A>G (p.Thr2428=) rs150845451 0.00019
NM_001374736.1(DST):c.2950C>T (p.Arg984Trp) rs138162782 0.00015
NM_001723.7(DST):c.7557G>A (p.Gln2519=) rs368876285 0.00014
NM_001374736.1(DST):c.3853A>G (p.Asn1285Asp) rs201419873 0.00012
NM_001374736.1(DST):c.3375G>A (p.Ala1125=) rs149789667 0.00011
NM_001374736.1(DST):c.4930-984G>A rs77216326 0.00011
NM_001374736.1(DST):c.4390C>T (p.Arg1464Trp) rs200316560 0.00010
NM_001374736.1(DST):c.4831-6T>A rs751953259 0.00010
NM_001374736.1(DST):c.4930-460A>G rs886061641 0.00010
NM_001374736.1(DST):c.2719C>T (p.Arg907Trp) rs775464446 0.00009
NM_001723.7(DST):c.4397A>G (p.Lys1466Arg) rs144279221 0.00007
NM_001374736.1(DST):c.1779-350C>T rs182565183 0.00006
NM_001374736.1(DST):c.4930-620A>C rs886061642 0.00006
NM_001723.7(DST):c.3715C>T (p.Arg1239Cys) rs371231287 0.00006
NM_001723.7(DST):c.3956C>A (p.Ala1319Glu) rs142302277 0.00006
NM_001723.7(DST):c.3957A>C (p.Ala1319=) rs543767625 0.00006
NM_001723.7(DST):c.7495C>T (p.Arg2499Trp) rs369328276 0.00006
NM_001723.7(DST):c.5346T>A (p.Leu1782=) rs769786699 0.00005
NM_001374736.1(DST):c.3600T>C (p.Ile1200=) rs200453699 0.00004
NM_001374736.1(DST):c.4380G>A (p.Thr1460=) rs200169945 0.00003
NM_001374736.1(DST):c.4750C>T (p.Arg1584Trp) rs200735287 0.00003
NM_001374736.1(DST):c.4930-428G>A rs886061640 0.00003
NM_001723.7(DST):c.7580T>C (p.Ile2527Thr) rs754471163 0.00003
NM_001374736.1(DST):c.1779-287A>T rs754357722 0.00002
NM_001723.7(DST):c.3690C>T (p.Ala1230=) rs374143007 0.00002
NM_001723.7(DST):c.5059G>A (p.Glu1687Lys) rs886061646 0.00002
NM_001723.7(DST):c.6673T>C (p.Leu2225=) rs753017821 0.00002
NM_001723.7(DST):c.7619A>G (p.Glu2540Gly) rs372196234 0.00002
NM_001374736.1(DST):c.1899G>A (p.Val633=) rs746002438 0.00001
NM_001374736.1(DST):c.3154C>G (p.His1052Asp) rs767323555 0.00001
NM_001374736.1(DST):c.3857T>G (p.Ile1286Ser) rs886061649 0.00001
NM_001723.7(DST):c.4050G>A (p.Thr1350=) rs377356403 0.00001
NM_001723.7(DST):c.4110A>G (p.Glu1370=) rs571317621 0.00001
NM_001723.7(DST):c.4464C>T (p.Asp1488=) rs80337136 0.00001
NM_001723.7(DST):c.4972A>G (p.Asn1658Asp) rs886061647 0.00001
NM_001723.7(DST):c.6007G>A (p.Ala2003Thr) rs74874398 0.00001
NM_001723.7(DST):c.6240T>G (p.Cys2080Trp) rs199558360 0.00001
NM_001723.7(DST):c.7224G>T (p.Glu2408Asp) rs769369001 0.00001
NM_001723.7(DST):c.7909C>A (p.Pro2637Thr) rs763986013 0.00001
NM_001374736.1(DST):c.1217C>T (p.Pro406Leu) rs1563465064
NM_001374736.1(DST):c.2620A>T (p.Ile874Phe) rs774974326
NM_001374736.1(DST):c.3283T>G (p.Cys1095Gly) rs886061650
NM_001374736.1(DST):c.4930-438G>C rs145471325
NM_001374736.1(DST):c.4930-771dup rs3841165
NM_001374736.1(DST):c.4930-772_4930-771dup rs3841165
NM_001723.7(DST):c.4090C>G (p.Leu1364Val) rs886061648
NM_001723.7(DST):c.4734G>A (p.Glu1578=) rs545103567
NM_001723.7(DST):c.5257G>A (p.Glu1753Lys) rs886061645
NM_001723.7(DST):c.5892C>T (p.Thr1964=) rs146263203
NM_001723.7(DST):c.6877C>T (p.Pro2293Ser) rs886061644
NM_001723.7(DST):c.6994A>C (p.Asn2332His) rs886061643

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