ClinVar Miner

List of variants in gene SLC16A1 reported as uncertain significance for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NC_000001.11:g.112956204G>C
NC_000001.11:g.112956208C>T
NC_000001.11:g.112956306C>T
NC_000001.11:g.112956314A>C
NM_003051.3(SLC16A1):c.*1018T>G rs774371594
NM_003051.3(SLC16A1):c.*104C>T rs182505461
NM_003051.3(SLC16A1):c.*1051G>A rs886045064
NM_003051.3(SLC16A1):c.*1064G>T rs886045063
NM_003051.3(SLC16A1):c.*1072G>T rs886045062
NM_003051.3(SLC16A1):c.*1312G>C rs886045059
NM_003051.3(SLC16A1):c.*1801A>G rs750135904
NM_003051.3(SLC16A1):c.*516C>G rs754537571
NM_003051.3(SLC16A1):c.*603T>C rs527658261
NM_003051.3(SLC16A1):c.*629C>T rs540946001
NM_003051.3(SLC16A1):c.*739T>G rs570060559
NM_003051.3(SLC16A1):c.*77C>T rs868304120
NM_003051.3(SLC16A1):c.*815G>A rs556305447
NM_003051.3(SLC16A1):c.*948G>A rs543171131
NM_003051.3(SLC16A1):c.-163T>C rs886045088
NM_003051.3(SLC16A1):c.-201T>A rs753315328
NM_003051.3(SLC16A1):c.-226G>A rs886045089
NM_003051.3(SLC16A1):c.-248G>T rs762453730
NM_003051.3(SLC16A1):c.-249C>T rs60953496
NM_003051.3(SLC16A1):c.-313T>C rs886045090
NM_003051.3(SLC16A1):c.-314A>G rs886045091
NM_003051.3(SLC16A1):c.-349G>A rs750771668
NM_003051.3(SLC16A1):c.-360G>A rs758825428
NM_003051.3(SLC16A1):c.-87C>T rs886045087
NM_003051.3(SLC16A1):c.-92G>T rs144301005
NM_003051.3(SLC16A1):c.1117G>A (p.Val373Ile) rs200802632
NM_003051.3(SLC16A1):c.1228+6G>A rs190615745
NM_003051.3(SLC16A1):c.1342T>C (p.Leu448=) rs773196238
NM_003051.3(SLC16A1):c.1345G>A (p.Ala449Thr) rs756006376
NM_003051.3(SLC16A1):c.1430T>C (p.Val477Ala) rs886045067
NM_003051.3(SLC16A1):c.1452G>A (p.Pro484=) rs17852382
NM_003051.3(SLC16A1):c.441C>T (p.Asn147=) rs150246870
NM_003051.3(SLC16A1):c.489C>A (p.Pro163=) rs145916504
NM_003051.3(SLC16A1):c.508G>A (p.Gly170Ser) rs200143982
NM_003051.3(SLC16A1):c.527G>A (p.Gly176Glu) rs766830652
NM_003051.3(SLC16A1):c.72T>A (p.Ile24=) rs760137043
NM_003051.3(SLC16A1):c.979C>T (p.Pro327Ser) rs77373295
NM_003051.3(SLC16A1):c.983G>T (p.Arg328Leu) rs774823539
NM_003051.4(SLC16A1):c.*1044T>G
NM_003051.4(SLC16A1):c.*1071T>C
NM_003051.4(SLC16A1):c.*1134G>A
NM_003051.4(SLC16A1):c.*137A>T
NM_003051.4(SLC16A1):c.*1654A>G
NM_003051.4(SLC16A1):c.*361G>T
NM_003051.4(SLC16A1):c.*657C>A
NM_003051.4(SLC16A1):c.*739T>C
NM_003051.4(SLC16A1):c.*946G>A
NM_003051.4(SLC16A1):c.1281C>T (p.Gly427=)
NM_003051.4(SLC16A1):c.1367A>T (p.Glu456Val)
NM_003051.4(SLC16A1):c.295G>A (p.Gly99Ser)
NM_003051.4(SLC16A1):c.540T>C (p.Ile180=)
NM_003051.4(SLC16A1):c.680A>G (p.His227Arg)

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