ClinVar Miner

List of variants in gene DST reported as pathogenic

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 118
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001723.7(DST):c.3383del (p.Ala1128fs) rs1426568243 0.00010
NM_001723.7(DST):c.3466C>T (p.Arg1156Ter) rs577972555 0.00006
NM_001723.7(DST):c.5086C>T (p.Arg1696Ter) rs528907932 0.00006
NM_001723.7(DST):c.3370C>T (p.Gln1124Ter) rs201045495 0.00004
NM_001723.7(DST):c.4720C>T (p.Gln1574Ter) rs1277472105 0.00004
NM_001723.7(DST):c.3748C>T (p.Arg1250Ter) rs779271284 0.00003
NM_001723.7(DST):c.4993C>T (p.Gln1665Ter) rs774625619 0.00003
NM_001723.7(DST):c.5854C>T (p.Gln1952Ter) rs755388186 0.00003
NM_001374736.1(DST):c.616C>T (p.Arg206Trp) rs374616412 0.00001
NM_001723.7(DST):c.4805T>G (p.Leu1602Ter) rs1487307181 0.00001
NM_001723.7(DST):c.5575C>T (p.Gln1859Ter) rs766044749 0.00001
NM_001374736.1(DST):c.10_19dup (p.Leu7fs) rs2127830414
NM_001374736.1(DST):c.12067C>T (p.Gln4023Ter)
NM_001374736.1(DST):c.12598del (p.Arg4200fs)
NM_001374736.1(DST):c.12720_12724del (p.Tyr4240_Lys4242delinsTer)
NM_001374736.1(DST):c.12924_12927delinsTA (p.Ser4309fs)
NM_001374736.1(DST):c.13149G>A (p.Trp4383Ter)
NM_001374736.1(DST):c.13478del (p.Phe4492_Leu4493insTer)
NM_001374736.1(DST):c.13707_13708insTAATATAAATAGAATAAAATAT (p.Thr4570Ter) rs2152610983
NM_001374736.1(DST):c.14057G>A (p.Trp4686Ter) rs2097544341
NM_001374736.1(DST):c.15158_15159del (p.Gln5053fs)
NM_001374736.1(DST):c.15216G>A (p.Trp5072Ter) rs893650971
NM_001374736.1(DST):c.15242dup (p.Asn5081fs)
NM_001374736.1(DST):c.15360del (p.Gly5121fs) rs2152556195
NM_001374736.1(DST):c.15529del (p.Thr5177fs)
NM_001374736.1(DST):c.16009C>T (p.Gln5337Ter)
NM_001374736.1(DST):c.16174C>T (p.Arg5392Ter) rs755738894
NM_001374736.1(DST):c.16435C>T (p.Arg5479Ter) rs2152554942
NM_001374736.1(DST):c.16536del (p.Glu5513fs)
NM_001374736.1(DST):c.16565_16566del (p.Gly5522fs)
NM_001374736.1(DST):c.16584_16587del (p.Asn5529fs)
NM_001374736.1(DST):c.16780C>T (p.Arg5594Ter) rs1198127456
NM_001374736.1(DST):c.16858del (p.Val5620fs) rs1584328172
NM_001374736.1(DST):c.16932del (p.Glu5645fs)
NM_001374736.1(DST):c.17053C>T (p.Gln5685Ter)
NM_001374736.1(DST):c.17251C>T (p.Gln5751Ter) rs2096867388
NM_001374736.1(DST):c.17452C>T (p.Gln5818Ter)
NM_001374736.1(DST):c.17779C>T (p.Gln5927Ter)
NM_001374736.1(DST):c.18008G>A (p.Trp6003Ter) rs2096799052
NM_001374736.1(DST):c.18061C>T (p.Arg6021Ter) rs777347824
NM_001374736.1(DST):c.18439C>T (p.Gln6147Ter) rs2152486042
NM_001374736.1(DST):c.18668del (p.Gly6223fs)
NM_001374736.1(DST):c.18715C>T (p.Gln6239Ter) rs2096469777
NM_001374736.1(DST):c.18818_18819dup (p.Arg6274fs)
NM_001374736.1(DST):c.19338dup (p.Ile6447fs)
NM_001374736.1(DST):c.19345A>T (p.Lys6449Ter) rs1562435373
NM_001374736.1(DST):c.19475_19478del (p.Asp6492fs)
NM_001374736.1(DST):c.19973C>G (p.Ser6658Ter)
NM_001374736.1(DST):c.20053dup (p.Thr6685fs) rs2095976276
NM_001374736.1(DST):c.20254G>T (p.Glu6752Ter) rs1480207376
NM_001374736.1(DST):c.20446C>T (p.Gln6816Ter) rs2095802050
NM_001374736.1(DST):c.20987_20988dup (p.Asp6997fs)
NM_001374736.1(DST):c.21233_21234insTTGGG (p.Arg7078fs)
NM_001374736.1(DST):c.21443G>A (p.Trp7148Ter)
NM_001374736.1(DST):c.21465_21466insTT (p.Leu7156fs)
NM_001374736.1(DST):c.2156C>G (p.Ser719Ter)
NM_001374736.1(DST):c.21756del (p.Ala7253fs) rs398122819
NM_001374736.1(DST):c.21862C>T (p.Gln7288Ter) rs2152409202
NM_001374736.1(DST):c.21985C>T (p.Arg7329Ter) rs2152403168
NM_001374736.1(DST):c.22005_22006insAT (p.Pro7336fs) rs2094929531
NM_001374736.1(DST):c.22203dup (p.Tyr7402fs)
NM_001374736.1(DST):c.22643G>A (p.Trp7548Ter)
NM_001374736.1(DST):c.22720G>T (p.Glu7574Ter) rs2152382691
NM_001374736.1(DST):c.22843C>T (p.Arg7615Ter) rs948596983
NM_001374736.1(DST):c.2386C>T (p.Arg796Ter) rs376491126
NM_001374736.1(DST):c.2989C>T (p.Gln997Ter)
NM_001374736.1(DST):c.3015C>A (p.Cys1005Ter) rs2152770295
NM_001374736.1(DST):c.3511C>T (p.Gln1171Ter)
NM_001374736.1(DST):c.364C>T (p.Arg122Ter) rs2127689099
NM_001374736.1(DST):c.3914del (p.Leu1305fs) rs2098784614
NM_001374736.1(DST):c.4016del (p.Asn1339fs) rs2152759509
NM_001374736.1(DST):c.4072C>T (p.Arg1358Ter) rs778397331
NM_001374736.1(DST):c.4083_4086dup (p.Val1363Ter) rs2152759445
NM_001374736.1(DST):c.4139del (p.Asp1380fs)
NM_001374736.1(DST):c.4651G>T (p.Glu1551Ter) rs375889300
NM_001374736.1(DST):c.4669_4670del (p.Ser1557fs) rs2152751675
NM_001374736.1(DST):c.4771C>T (p.Gln1591Ter)
NM_001374736.1(DST):c.4792C>T (p.Arg1598Ter) rs1188417345
NM_001374736.1(DST):c.4854_4855dup (p.Thr1619fs) rs2152746765
NM_001374736.1(DST):c.4924del (p.Glu1642fs)
NM_001374736.1(DST):c.5076dup (p.Ser1693fs) rs2098545189
NM_001374736.1(DST):c.5194_5195del (p.Leu1732fs)
NM_001374736.1(DST):c.5850del (p.Pro1950_Val1951insTer)
NM_001374736.1(DST):c.608C>A (p.Ala203Glu) rs201871537
NM_001374736.1(DST):c.687+1G>A rs1426972011
NM_001723.7(DST):c.3410del (p.Thr1137fs) rs2098681738
NM_001723.7(DST):c.3565del (p.Ala1189fs) rs2152739843
NM_001723.7(DST):c.3644_3648del (p.Glu1215fs) rs2098678320
NM_001723.7(DST):c.3655C>T (p.Gln1219Ter)
NM_001723.7(DST):c.3745A>T (p.Arg1249Ter) rs398122943
NM_001723.7(DST):c.4080dup (p.Ala1361fs)
NM_001723.7(DST):c.4096C>T (p.Gln1366Ter) rs770035646
NM_001723.7(DST):c.4152del (p.Glu1384fs)
NM_001723.7(DST):c.4189del (p.Thr1397fs)
NM_001723.7(DST):c.4189dup (p.Thr1397fs) rs772099949
NM_001723.7(DST):c.4262del (p.Lys1421fs)
NM_001723.7(DST):c.4477del (p.Ala1493fs) rs758599939
NM_001723.7(DST):c.4534C>T (p.Arg1512Ter) rs761229102
NM_001723.7(DST):c.4545dup (p.Glu1516fs)
NM_001723.7(DST):c.4554_4557del (p.Glu1518fs) rs748899221
NM_001723.7(DST):c.4763T>A (p.Leu1588Ter) rs780422336
NM_001723.7(DST):c.5078_5079del (p.Glu1693fs)
NM_001723.7(DST):c.5177dup (p.Thr1727fs) rs759006806
NM_001723.7(DST):c.5182del (p.Thr1727_Ile1728insTer)
NM_001723.7(DST):c.5221C>T (p.Gln1741Ter)
NM_001723.7(DST):c.5280del (p.Lys1760fs) rs1376812152
NM_001723.7(DST):c.5357del (p.Asn1786fs) rs1440037452
NM_001723.7(DST):c.5416C>T (p.Gln1806Ter) rs2098654029
NM_001723.7(DST):c.5449_5452dup (p.Gln1818fs)
NM_001723.7(DST):c.5484T>A (p.Cys1828Ter)
NM_001723.7(DST):c.5500dup (p.Glu1834fs)
NM_001723.7(DST):c.5729del (p.Pro1910fs)
NM_001723.7(DST):c.5874C>A (p.Tyr1958Ter)
NM_001723.7(DST):c.5949_5950del (p.Lys1984fs) rs2152733577
NM_001723.7(DST):c.6387dup (p.Asn2130Ter) rs2152731563
NM_001723.7(DST):c.7097dup (p.Tyr2366Ter) rs2152729916
NM_001723.7(DST):c.7429del (p.Leu2477fs) rs2152728832
NM_001723.7(DST):c.7543C>T (p.Gln2515Ter) rs1057524203

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.