ClinVar Miner

List of variants in gene GLDC reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 108
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HGVS dbSNP
NM_000170.2(GLDC):c.1278G>A (p.Gly426=) rs1554647023
NM_000170.2(GLDC):c.1331G>A (p.Cys444Tyr) rs142099123
NM_000170.2(GLDC):c.1453T>C (p.Leu485=) rs760562478
NM_000170.2(GLDC):c.1483-6C>T rs1442788186
NM_000170.2(GLDC):c.1618A>C (p.Lys540Gln) rs140516872
NM_000170.2(GLDC):c.1665+7A>T rs759573888
NM_000170.2(GLDC):c.1752T>C (p.Pro584=) rs150647379
NM_000170.2(GLDC):c.190G>T (p.Ala64Ser) rs141601131
NM_000170.2(GLDC):c.1927-4G>A rs576723612
NM_000170.2(GLDC):c.1932C>T (p.Cys644=) rs111348076
NM_000170.2(GLDC):c.2024A>C (p.Asn675Thr) rs749513146
NM_000170.2(GLDC):c.2126A>G (p.Asn709Ser) rs150943866
NM_000170.2(GLDC):c.2244G>A (p.Ser748=) rs372693840
NM_000170.2(GLDC):c.2283A>G (p.Gly761=) rs1554643744
NM_000170.2(GLDC):c.2304G>A (p.Gly768=) rs533775952
NM_000170.2(GLDC):c.2352C>T (p.Pro784=) rs367781728
NM_000170.2(GLDC):c.2409C>T (p.Ala803=) rs1554643608
NM_000170.2(GLDC):c.2487C>T (p.Ala829=) rs141806715
NM_000170.2(GLDC):c.2665+10T>C rs774684209
NM_000170.2(GLDC):c.2832G>A (p.Pro944=) rs764242927
NM_000170.2(GLDC):c.2964G>A (p.Arg988=) rs146045718
NM_000170.2(GLDC):c.2964G>C (p.Arg988=) rs146045718
NM_000170.2(GLDC):c.327C>T (p.Asp109=) rs1181706015
NM_000170.2(GLDC):c.40C>A (p.Arg14Ser) rs182760732
NM_000170.2(GLDC):c.619C>G (p.Leu207Val) rs142181803
NM_000170.2(GLDC):c.642C>T (p.Asn214=) rs775546889
NM_000170.3(GLDC):c.103C>A (p.Arg35=) rs764400486
NM_000170.3(GLDC):c.1080G>T (p.Val360=) rs745502236
NM_000170.3(GLDC):c.1149A>G (p.Thr383=) rs146499591
NM_000170.3(GLDC):c.114C>T (p.Ser38=) rs1315587398
NM_000170.3(GLDC):c.1155+9C>G rs994997633
NM_000170.3(GLDC):c.1161C>A (p.Leu387=) rs781613958
NM_000170.3(GLDC):c.1167G>C (p.Ala389=) rs199901045
NM_000170.3(GLDC):c.1210C>T (p.Leu404=) rs781450542
NM_000170.3(GLDC):c.1215G>A (p.Glu405=) rs771135075
NM_000170.3(GLDC):c.1242C>T (p.Ala414=) rs761471932
NM_000170.3(GLDC):c.1262-4G>A rs549797631
NM_000170.3(GLDC):c.1296C>T (p.Asp432=) rs766465179
NM_000170.3(GLDC):c.1311C>T (p.Thr437=) rs1317859936
NM_000170.3(GLDC):c.1332C>T (p.Cys444=) rs781050148
NM_000170.3(GLDC):c.1359C>T (p.Ala453=) rs766839627
NM_000170.3(GLDC):c.1401+9A>G rs75555848
NM_000170.3(GLDC):c.1428C>T (p.Val476=) rs781701911
NM_000170.3(GLDC):c.1446C>T (p.Asp482=) rs201147701
NM_000170.3(GLDC):c.147C>T (p.Ala49=) rs994081399
NM_000170.3(GLDC):c.1554G>A (p.Pro518=) rs377219563
NM_000170.3(GLDC):c.1554G>C (p.Pro518=) rs377219563
NM_000170.3(GLDC):c.1689C>T (p.Asn563=) rs546431385
NM_000170.3(GLDC):c.1740C>T (p.His580=) rs1587946346
NM_000170.3(GLDC):c.1791G>C (p.Glu597Asp)
NM_000170.3(GLDC):c.1797G>A (p.Glu599=) rs1587946274
NM_000170.3(GLDC):c.1850+7G>A rs1334727362
NM_000170.3(GLDC):c.1851-9C>G rs377751310
NM_000170.3(GLDC):c.1851C>T (p.Ser617=) rs777724341
NM_000170.3(GLDC):c.1893C>T (p.Ala631=) rs565751857
NM_000170.3(GLDC):c.190G>A (p.Ala64Thr) rs141601131
NM_000170.3(GLDC):c.1926+6T>C rs200007891
NM_000170.3(GLDC):c.1941G>A (p.Pro647=) rs1232468588
NM_000170.3(GLDC):c.1953T>C (p.His651=) rs777613879
NM_000170.3(GLDC):c.1974C>A (p.Ala658=) rs534062853
NM_000170.3(GLDC):c.2052+7G>C rs755812288
NM_000170.3(GLDC):c.2073C>T (p.Asn691=) rs140352381
NM_000170.3(GLDC):c.2097C>T (p.Tyr699=) rs149694787
NM_000170.3(GLDC):c.2127C>T (p.Asn709=) rs753895623
NM_000170.3(GLDC):c.2160T>C (p.His720=) rs758841885
NM_000170.3(GLDC):c.2175C>T (p.Tyr725=) rs147951756
NM_000170.3(GLDC):c.2202+8C>A rs577906178
NM_000170.3(GLDC):c.2211C>T (p.Ile737=) rs1587923448
NM_000170.3(GLDC):c.2229C>T (p.Phe743=) rs144317480
NM_000170.3(GLDC):c.2256T>C (p.Leu752=) rs1587923380
NM_000170.3(GLDC):c.2271C>T (p.Cys757=) rs770961258
NM_000170.3(GLDC):c.2307C>T (p.Pro769=) rs565834029
NM_000170.3(GLDC):c.2310C>T (p.Ile770=) rs765661419
NM_000170.3(GLDC):c.2315+8C>T rs773354023
NM_000170.3(GLDC):c.2328C>T (p.Leu776=) rs149600380
NM_000170.3(GLDC):c.2352C>G (p.Pro784=) rs367781728
NM_000170.3(GLDC):c.2406G>A (p.Ala802=) rs368811775
NM_000170.3(GLDC):c.255+8C>T rs202086134
NM_000170.3(GLDC):c.2565A>C (p.Ala855=) rs966395392
NM_000170.3(GLDC):c.258C>T (p.Ser86=) rs562000292
NM_000170.3(GLDC):c.2601G>A (p.Thr867=) rs371678175
NM_000170.3(GLDC):c.261T>C (p.Ile87=) rs776700682
NM_000170.3(GLDC):c.2683A>G rs141152043
NM_000170.3(GLDC):c.2703G>C (p.Gly901=) rs369767254
NM_000170.3(GLDC):c.2718G>A (p.Glu906=) rs1463086398
NM_000170.3(GLDC):c.2793T>A (p.Ala931=) rs367759326
NM_000170.3(GLDC):c.2821A>C (p.Arg941=) rs1587909520
NM_000170.3(GLDC):c.282G>C (p.Thr94=) rs769003941
NM_000170.3(GLDC):c.2838+10C>T rs1587909491
NM_000170.3(GLDC):c.2863G>A (p.Val955Ile) rs148540696
NM_000170.3(GLDC):c.2874C>T (p.Ser958=) rs146339375
NM_000170.3(GLDC):c.3002C>A (p.Thr1001Asn) rs555776146
NM_000170.3(GLDC):c.396G>T (p.Ser132=) rs542613459
NM_000170.3(GLDC):c.470+8A>G rs1428962515
NM_000170.3(GLDC):c.471-10T>A rs369391624
NM_000170.3(GLDC):c.489A>G (p.Pro163=) rs770044310
NM_000170.3(GLDC):c.51G>T (p.Gly17=) rs947785805
NM_000170.3(GLDC):c.576C>G (p.Ala192=) rs768514155
NM_000170.3(GLDC):c.582A>G (p.Ala194=) rs1587964992
NM_000170.3(GLDC):c.609C>T (p.Ala203=) rs201699152
NM_000170.3(GLDC):c.714-4C>G rs1206369229
NM_000170.3(GLDC):c.78G>C (p.Ser26=) rs915226152
NM_000170.3(GLDC):c.81G>A (p.Gly27=) rs1457809070
NM_000170.3(GLDC):c.831G>A (p.Thr277=) rs369824891
NM_000170.3(GLDC):c.84G>T (p.Pro28=) rs1259938806
NM_000170.3(GLDC):c.862-7T>G rs761854548
NM_000170.3(GLDC):c.96G>T (p.Pro32=) rs1430526811
NM_000170.3(GLDC):c.972G>A (p.Leu324=) rs754536865

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