ClinVar Miner

List of variants in gene DST reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 135
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HGVS dbSNP gnomAD frequency
NM_001374736.1(DST):c.20997G>A (p.Leu6999=) rs187652380 0.00781
NM_001374736.1(DST):c.13820C>A (p.Pro4607His) rs138967674 0.00744
NM_001723.7(DST):c.5780A>G (p.His1927Arg) rs12209266 0.00441
NM_001374736.1(DST):c.10443G>A (p.Thr3481=) rs45498096 0.00379
NM_001723.7(DST):c.3336G>C (p.Glu1112Asp) rs34767818 0.00349
NM_001374736.1(DST):c.12839A>G (p.Lys4280Arg) rs186813964 0.00285
NM_001374736.1(DST):c.4929+81A>G rs542262570 0.00280
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_001723.7(DST):c.25C>T (p.Arg9Cys) rs75671065 0.00193
NM_001374736.1(DST):c.22916C>T (p.Ala7639Val) rs201429821 0.00178
NM_001374736.1(DST):c.2350C>G (p.Pro784Ala) rs151271595 0.00152
NM_001374736.1(DST):c.2705C>G (p.Ser902Cys) rs138553142 0.00148
NM_001374736.1(DST):c.21538A>G (p.Met7180Val) rs200006386 0.00141
NM_001723.7(DST):c.7135G>A (p.Ala2379Thr) rs140192373 0.00140
NM_001723.7(DST):c.4049C>T (p.Thr1350Met) rs45472691 0.00137
NM_001374736.1(DST):c.21423G>A (p.Val7141=) rs201115435 0.00133
NM_001374736.1(DST):c.4929+3811G>A rs146628688 0.00121
NM_001374736.1(DST):c.742A>G (p.Ile248Val) rs112635185 0.00121
NM_001374736.1(DST):c.4997A>T (p.Asn1666Ile) rs183804748 0.00118
NM_001374736.1(DST):c.258A>G (p.Ala86=) rs201106926 0.00115
NM_001723.7(DST):c.6582A>C (p.Ala2194=) rs149007397 0.00115
NM_001374736.1(DST):c.18433C>T (p.Arg6145Trp) rs193252082 0.00107
NM_001374736.1(DST):c.16495A>T (p.Ser5499Cys) rs180765536 0.00102
NM_001374736.1(DST):c.16967G>A (p.Arg5656Gln) rs116774070 0.00088
NM_001374736.1(DST):c.15309T>A (p.Phe5103Leu) rs191081991 0.00086
NM_001723.7(DST):c.3436A>G (p.Met1146Val) rs148413592 0.00066
NM_001374736.1(DST):c.20976C>T (p.Asn6992=) rs199658821 0.00064
NM_001374736.1(DST):c.11542-8C>T rs370887046 0.00060
NM_001374736.1(DST):c.12043A>T (p.Ile4015Phe) rs201249286 0.00057
NM_001374736.1(DST):c.15570G>A (p.Glu5190=) rs200941177 0.00052
NM_001723.7(DST):c.6868A>G (p.Arg2290Gly) rs112473525 0.00047
NM_001374736.1(DST):c.16047C>G (p.Thr5349=) rs370841140 0.00041
NM_001374736.1(DST):c.4638+7A>T rs185349093 0.00041
NM_001374736.1(DST):c.12159T>G (p.Thr4053=) rs369432519 0.00035
NM_001374736.1(DST):c.3282C>T (p.Asp1094=) rs145723100 0.00034
NM_001374736.1(DST):c.5148-8T>C rs376856354 0.00034
NM_001723.7(DST):c.7578G>A (p.Gly2526=) rs143623628 0.00032
NM_001374736.1(DST):c.4046C>T (p.Ala1349Val) rs150656535 0.00029
NM_001723.7(DST):c.5095G>A (p.Glu1699Lys) rs201526616 0.00029
NM_001723.7(DST):c.6831C>T (p.Ala2277=) rs34628660 0.00029
NM_001374736.1(DST):c.23055C>T (p.Pro7685=) rs201991278 0.00025
NM_001374736.1(DST):c.14441-7C>T rs41271866 0.00022
NM_001374736.1(DST):c.19656G>C (p.Glu6552Asp) rs199549741 0.00021
NM_001723.7(DST):c.7284A>G (p.Thr2428=) rs150845451 0.00019
NM_001374736.1(DST):c.22458C>T (p.Ala7486=) rs554828969 0.00018
NM_001374736.1(DST):c.17450A>G (p.Gln5817Arg) rs761791970 0.00017
NM_001374736.1(DST):c.20148G>A (p.Thr6716=) rs552952660 0.00016
NM_001374736.1(DST):c.133G>A (p.Gly45Arg) rs139905357 0.00012
NM_001374736.1(DST):c.23405C>T (p.Thr7802Met) rs367598583 0.00011
NM_001374736.1(DST):c.2757G>A (p.Ala919=) rs376863860 0.00011
NM_001374736.1(DST):c.3375G>A (p.Ala1125=) rs149789667 0.00011
NM_001374736.1(DST):c.12549C>T (p.Asp4183=) rs375624981 0.00009
NM_001374736.1(DST):c.12959C>T (p.Thr4320Met) rs544327450 0.00009
NM_001374736.1(DST):c.16922C>T (p.Ala5641Val) rs768150254 0.00009
NM_001374736.1(DST):c.13722-4G>A rs190649369 0.00008
NM_001374736.1(DST):c.14495A>G (p.Glu4832Gly) rs201437391 0.00008
NM_001374736.1(DST):c.15902C>T (p.Ser5301Leu) rs112177059 0.00008
NM_001374736.1(DST):c.20412T>C (p.Ala6804=) rs146563577 0.00008
NM_001374736.1(DST):c.4120A>G (p.Met1374Val) rs138508306 0.00008
NM_001374736.1(DST):c.12238A>G (p.Ile4080Val) rs200855949 0.00007
NM_001374736.1(DST):c.13499T>C (p.Leu4500Pro) rs758532940 0.00006
NM_001374736.1(DST):c.17340G>A (p.Lys5780=) rs200304225 0.00006
NM_001374736.1(DST):c.21885C>T (p.Thr7295=) rs764924172 0.00004
NM_001374736.1(DST):c.3699T>C (p.Asp1233=) rs751682343 0.00004
NM_001723.7(DST):c.6415A>G (p.Ile2139Val) rs374067079 0.00004
NM_001374736.1(DST):c.16233G>C (p.Val5411=) rs201830030 0.00003
NM_001374736.1(DST):c.16747C>T (p.Arg5583Trp) rs568055144 0.00003
NM_001374736.1(DST):c.2534T>G (p.Val845Gly) rs776991432 0.00003
NM_001374736.1(DST):c.11679T>C (p.Tyr3893=) rs375258425 0.00002
NM_001374736.1(DST):c.22377T>C (p.Asp7459=) rs757599796 0.00002
NM_001723.7(DST):c.4020C>T (p.Ile1340=) rs768554069 0.00002
NM_001374736.1(DST):c.18072C>T (p.Ser6024=) rs747333827 0.00001
NM_001374736.1(DST):c.18358A>G (p.Lys6120Glu) rs2096572467 0.00001
NM_001374736.1(DST):c.3477G>A (p.Ala1159=) rs201509973 0.00001
NM_001374736.1(DST):c.4833C>G (p.Phe1611Leu) rs1563270846 0.00001
NM_001374736.1(DST):c.5199G>A (p.Gln1733=) rs552582917 0.00001
NM_001723.7(DST):c.5586G>A (p.Leu1862=) rs762547836 0.00001
NM_001374736.1(DST):c.10206A>G (p.Ala3402=)
NM_001374736.1(DST):c.10475T>A (p.Ile3492Asn)
NM_001374736.1(DST):c.10546T>C (p.Cys3516Arg)
NM_001374736.1(DST):c.10684T>C (p.Leu3562=)
NM_001374736.1(DST):c.10954G>A (p.Gly3652Arg)
NM_001374736.1(DST):c.109T>C (p.Cys37Arg)
NM_001374736.1(DST):c.11139T>G (p.Leu3713=)
NM_001374736.1(DST):c.11223A>G (p.Ser3741=)
NM_001374736.1(DST):c.11514T>C (p.His3838=)
NM_001374736.1(DST):c.11634A>G (p.Gln3878=)
NM_001374736.1(DST):c.11842T>G (p.Cys3948Gly) rs1554449844
NM_001374736.1(DST):c.12218C>T (p.Ser4073Phe) rs1277292455
NM_001374736.1(DST):c.12703C>T (p.Arg4235Trp) rs778888568
NM_001374736.1(DST):c.13200C>T (p.Asn4400=) rs2097816389
NM_001374736.1(DST):c.13701G>A (p.Met4567Ile) rs1445711960
NM_001374736.1(DST):c.13825G>A (p.Val4609Ile) rs1031797194
NM_001374736.1(DST):c.14367A>G (p.Lys4789=) rs1203098297
NM_001374736.1(DST):c.1545A>G (p.Val515=)
NM_001374736.1(DST):c.15903G>A (p.Ser5301=) rs371189011
NM_001374736.1(DST):c.16074C>T (p.Thr5358=)
NM_001374736.1(DST):c.16834C>T (p.Leu5612=)
NM_001374736.1(DST):c.1686A>G (p.Gln562=)
NM_001374736.1(DST):c.16896G>A (p.Pro5632=)
NM_001374736.1(DST):c.17016A>C (p.Thr5672=)
NM_001374736.1(DST):c.17497C>G (p.Leu5833Val) rs1584163798
NM_001374736.1(DST):c.17854G>T (p.Glu5952Ter) rs1341890249
NM_001374736.1(DST):c.18329G>A (p.Cys6110Tyr)
NM_001374736.1(DST):c.18417G>T (p.Arg6139Ser) rs1057519122
NM_001374736.1(DST):c.19238A>T (p.Glu6413Val) rs1583469392
NM_001374736.1(DST):c.19369T>G (p.Ser6457Ala) rs2152468178
NM_001374736.1(DST):c.19419T>G (p.Leu6473=)
NM_001374736.1(DST):c.20657A>G (p.Lys6886Arg)
NM_001374736.1(DST):c.20916C>T (p.Tyr6972=) rs763815018
NM_001374736.1(DST):c.20987_20988dup (p.Asp6997fs)
NM_001374736.1(DST):c.21651A>T (p.Thr7217=)
NM_001374736.1(DST):c.21663G>A (p.Ala7221=)
NM_001374736.1(DST):c.2181T>A (p.Pro727=) rs2152777551
NM_001374736.1(DST):c.22314T>C (p.Leu7438=)
NM_001374736.1(DST):c.3986G>A (p.Arg1329Gln) rs763518239
NM_001374736.1(DST):c.414G>A (p.Arg138=)
NM_001374736.1(DST):c.4435G>A (p.Val1479Ile)
NM_001374736.1(DST):c.4929+39G>A
NM_001374736.1(DST):c.5259A>C (p.Ser1753=)
NM_001374736.1(DST):c.528C>G (p.Thr176=)
NM_001374736.1(DST):c.5574T>C (p.Ala1858=)
NM_001374736.1(DST):c.5858C>T (p.Pro1953Leu)
NM_001374736.1(DST):c.588G>A (p.Val196=)
NM_001374736.1(DST):c.6220T>C (p.Trp2074Arg)
NM_001374736.1(DST):c.6302T>C (p.Leu2101Pro)
NM_001374736.1(DST):c.6421A>G (p.Ile2141Val)
NM_001374736.1(DST):c.6510C>G (p.Pro2170=)
NM_001374736.1(DST):c.6666C>T (p.Tyr2222=)
NM_001374736.1(DST):c.8340C>T (p.Ser2780=)
NM_001723.7(DST):c.22del (p.Tyr8fs) rs775912185
NM_001723.7(DST):c.3448C>T (p.Leu1150=)
NM_001723.7(DST):c.5892C>T (p.Thr1964=) rs146263203

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