ClinVar Miner

List of variants in gene AGL reported as benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP
NM_000642.3(AGL):c.*1028C>T rs3766601
NM_000642.3(AGL):c.*1244T>A rs72963791
NM_000642.3(AGL):c.*1296A>C rs1804809
NM_000642.3(AGL):c.*1541T>C rs3766603
NM_000642.3(AGL):c.*272G>T rs1804808
NM_000642.3(AGL):c.*575G>T rs60880558
NM_000642.3(AGL):c.*732C>T rs3766600
NM_000642.3(AGL):c.*739A>G rs41285742
NM_000642.3(AGL):c.-10A>G rs2307130
NM_000642.3(AGL):c.112A>G (p.Thr38Ala) rs35278779
NM_000642.3(AGL):c.1155G>T (p.Lys385Asn) rs28730701
NM_000642.3(AGL):c.1160G>A (p.Arg387Gln) rs17121464
NM_000642.3(AGL):c.1185+15T>C rs17121466
NM_000642.3(AGL):c.1283+13del
NM_000642.3(AGL):c.1319C>T (p.Ser440Phe) rs149771710
NM_000642.3(AGL):c.1481G>A (p.Arg494His) rs141043166
NM_000642.3(AGL):c.1602C>T (p.His534=) rs563472929
NM_000642.3(AGL):c.1611+11del
NM_000642.3(AGL):c.1759C>T (p.His587Tyr) rs139488862
NM_000642.3(AGL):c.1875G>T (p.Thr625=) rs141944878
NM_000642.3(AGL):c.1880A>G (p.Asp627Gly)
NM_000642.3(AGL):c.2001+8T>C rs3736296
NM_000642.3(AGL):c.207T>C (p.Asn69=) rs2230305
NM_000642.3(AGL):c.2192C>T (p.Ala731Val)
NM_000642.3(AGL):c.2280C>T (p.Ser760=) rs373513564
NM_000642.3(AGL):c.2522C>T (p.Ser841Phe) rs150441555
NM_000642.3(AGL):c.2546+10T>C rs74551473
NM_000642.3(AGL):c.2802A>C (p.Ala934=) rs34230588
NM_000642.3(AGL):c.2812+11G>A rs555929
NM_000642.3(AGL):c.2883A>G (p.Arg961=) rs113625417
NM_000642.3(AGL):c.2885C>G (p.Ser962Cys) rs34714252
NM_000642.3(AGL):c.3084-8T>C rs186402161
NM_000642.3(AGL):c.3199C>T (p.Pro1067Ser) rs3753494
NM_000642.3(AGL):c.3203A>G (p.Tyr1068Cys) rs147165298
NM_000642.3(AGL):c.3260-19G>A rs140333425
NM_000642.3(AGL):c.3343G>A (p.Gly1115Arg) rs2230307
NM_000642.3(AGL):c.3384G>A (p.Ala1128=) rs149393587
NM_000642.3(AGL):c.3431T>A (p.Ile1144Asn) rs2230308
NM_000642.3(AGL):c.3619G>A (p.Ala1207Thr) rs11807956
NM_000642.3(AGL):c.3758G>A (p.Arg1253His) rs12043139
NM_000642.3(AGL):c.3792A>T (p.Gly1264=) rs148606237
NM_000642.3(AGL):c.3849T>C (p.Ala1283=) rs28730706
NM_000642.3(AGL):c.39C>T (p.Asn13=) rs138203039
NM_000642.3(AGL):c.4027G>A (p.Glu1343Lys) rs112795811
NM_000642.3(AGL):c.4162-11G>A rs184309460
NM_000642.3(AGL):c.4331A>G (p.Asn1444Ser) rs143815159
NM_000642.3(AGL):c.4430C>G (p.Thr1477Ser) rs78348923
NM_000642.3(AGL):c.686A>G (p.Gln229Arg) rs17121403
NM_000642.3(AGL):c.894C>T (p.Leu298=) rs2230306
NM_000642.3(AGL):c.959-18G>A rs634880

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