ClinVar Miner

List of variants in gene GLDC reported by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP
NM_000170.2(GLDC):c.*115A>T rs148273307
NM_000170.2(GLDC):c.*188C>T rs577665662
NM_000170.2(GLDC):c.*235T>G rs749941145
NM_000170.2(GLDC):c.*257G>A rs111326356
NM_000170.2(GLDC):c.*410G>C rs35834773
NM_000170.2(GLDC):c.*473C>T rs1061407
NM_000170.2(GLDC):c.*505_*506delTT rs3215922
NM_000170.2(GLDC):c.*540C>T rs7848919
NM_000170.2(GLDC):c.*546C>T rs768890473
NM_000170.2(GLDC):c.*557C>G rs73639311
NM_000170.2(GLDC):c.*5C>G rs764814250
NM_000170.2(GLDC):c.*7G>C rs2228098
NM_000170.2(GLDC):c.-168G>A rs891076552
NM_000170.2(GLDC):c.-173T>G rs1039584725
NM_000170.2(GLDC):c.-186delC rs140030144
NM_000170.2(GLDC):c.-21C>T rs1057515609
NM_000170.2(GLDC):c.1000T>C (p.Phe334Leu) rs149133229
NM_000170.2(GLDC):c.1156-7C>G rs150095531
NM_000170.2(GLDC):c.1166C>T (p.Ala389Val) rs121964979
NM_000170.2(GLDC):c.1229G>A (p.Arg410Lys) rs144090917
NM_000170.2(GLDC):c.1357G>T (p.Ala453Ser) rs1057515607
NM_000170.2(GLDC):c.1384C>G (p.Leu462Val) rs73400312
NM_000170.2(GLDC):c.1424C>T (p.Thr475Ile) rs750883330
NM_000170.2(GLDC):c.142G>T (p.Gly48Trp) rs1057515608
NM_000170.2(GLDC):c.1483-15G>C rs371777070
NM_000170.2(GLDC):c.150G>A (p.Ser50=) rs768354829
NM_000170.2(GLDC):c.1545G>C (p.Arg515Ser) rs121964976
NM_000170.2(GLDC):c.1553C>A (p.Pro518Gln) rs761064507
NM_000170.2(GLDC):c.1580+5G>T rs764790596
NM_000170.2(GLDC):c.1581-5C>T rs184463452
NM_000170.2(GLDC):c.1626A>G (p.Glu542=) rs779537709
NM_000170.2(GLDC):c.1707+8G>A rs144666843
NM_000170.2(GLDC):c.1815C>T (p.Leu605=) rs74461075
NM_000170.2(GLDC):c.1927-9A>G rs41281773
NM_000170.2(GLDC):c.1940C>T (p.Pro647Leu) rs201135624
NM_000170.2(GLDC):c.2147T>A (p.Leu716His) rs145018304
NM_000170.2(GLDC):c.2149A>G (p.Ile717Val) rs117460214
NM_000170.2(GLDC):c.2203G>T (p.Val735Leu) rs143119940
NM_000170.2(GLDC):c.2316-6dupA rs3215923
NM_000170.2(GLDC):c.249G>A (p.Gly83=) rs12341698
NM_000170.2(GLDC):c.2518A>G (p.Met840Val) rs781693346
NM_000170.2(GLDC):c.2564C>T (p.Ala855Val) rs764251972
NM_000170.2(GLDC):c.2650A>G (p.Arg884Gly) rs1057515606
NM_000170.2(GLDC):c.2683A>G (p.Met895Val) rs141152043
NM_000170.2(GLDC):c.2730G>A (p.Ser910=) rs144937031
NM_000170.2(GLDC):c.2748G>A (p.Leu916=) rs139982267
NM_000170.2(GLDC):c.2919+3A>G rs73639325
NM_000170.2(GLDC):c.2919C>T (p.Leu973=) rs113736090
NM_000170.2(GLDC):c.2947T>C (p.Trp983Arg) rs1057515605
NM_000170.2(GLDC):c.2988G>C (p.Gln996His) rs138640017
NM_000170.2(GLDC):c.319A>G (p.Met107Val) rs138454333
NM_000170.2(GLDC):c.438G>A (p.Thr146=) rs13289273
NM_000170.2(GLDC):c.470+11T>C rs142534180
NM_000170.2(GLDC):c.501G>A (p.Glu167=) rs35374927
NM_000170.2(GLDC):c.52G>T (p.Gly18Cys) rs535143891
NM_000170.2(GLDC):c.63C>A (p.Arg21=) rs372141443
NM_000170.2(GLDC):c.660C>T (p.Leu220=) rs2228095
NM_000170.2(GLDC):c.666T>C (p.Asp222=) rs12004164
NM_000170.2(GLDC):c.671G>A (p.Arg224His) rs28617412
NM_000170.2(GLDC):c.698T>C (p.Val233Ala) rs140013612
NM_000170.2(GLDC):c.701A>G (p.Gln234Arg) rs776639131
NM_000170.2(GLDC):c.871T>G (p.Cys291Gly) rs141014950

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