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Variants search result for Homo sapiens
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35 records found for search term Slc35f5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156389105CV2373537single nucleotide variantNM_025181.5(SLC35F5):c.83A>C (p.Lys28Thr)not specified [RCV004222643]uncertain significance2113755502113755502Humanname
156200508CV2392401single nucleotide variantNM_025181.5(SLC35F5):c.91G>A (p.Gly31Ser)not specified [RCV004243984]uncertain significance2113755494113755494Humanname
597702533CV3599730single nucleotide variantNM_025181.5(SLC35F5):c.35G>A (p.Arg12Lys)not specified [RCV004860100]uncertain significance2113756375113756375Humanname
597765676CV3599736single nucleotide variantNM_025181.5(SLC35F5):c.49A>T (p.Ser17Cys)not specified [RCV004870375]uncertain significance2113755536113755536Humanname
155935910CV2380157single nucleotide variantNM_025181.5(SLC35F5):c.293A>G (p.Asn98Ser)not specified [RCV004224528]uncertain significance2113750549113750549Humanname
156044950CV2381680single nucleotide variantNM_025181.5(SLC35F5):c.197G>A (p.Arg66His)not specified [RCV004232146]uncertain significance2113755241113755241Humanname
405784845CV3332804single nucleotide variantNM_025181.5(SLC35F5):c.284C>T (p.Thr95Ile)not specified [RCV004459322]uncertain significance2113750558113750558Humanname
407510141CV3484472single nucleotide variantNM_025181.5(SLC35F5):c.138A>C (p.Gln46His)not specified [RCV004672627]uncertain significance2113755300113755300Humanname
407510147CV3484474single nucleotide variantNM_025181.5(SLC35F5):c.148G>C (p.Val50Leu)not specified [RCV004672629]uncertain significance2113755290113755290Humanname
597765801CV3599734single nucleotide variantNM_025181.5(SLC35F5):c.177G>C (p.Gln59His)not specified [RCV004870374]uncertain significance2113755261113755261Humanname
597702554CV3599735single nucleotide variantNM_025181.5(SLC35F5):c.221T>G (p.Val74Gly)not specified [RCV004860102]uncertain significance2113755217113755217Humanname
598242971CV3914832single nucleotide variantNM_025181.5(SLC35F5):c.257C>G (p.Ser86Cys)not specified [RCV005276625]uncertain significance2113755181113755181Humanname
598242978CV3914833single nucleotide variantNM_025181.5(SLC35F5):c.221T>C (p.Val74Ala)not specified [RCV005276626]uncertain significance2113755217113755217Humanname
598242984CV3914834single nucleotide variantNM_025181.5(SLC35F5):c.157A>G (p.Met53Val)not specified [RCV005276627]uncertain significance2113755281113755281Humanname
156063798CV2228826single nucleotide variantNM_025181.5(SLC35F5):c.964C>T (p.Pro322Ser)not specified [RCV004095069]likely benign2113731605113731605Humanname
156257178CV2307860single nucleotide variantNM_025181.5(SLC35F5):c.566C>T (p.Pro189Leu)not specified [RCV004170320]uncertain significance2113742876113742876Humanname
156165984CV2319906single nucleotide variantNM_025181.5(SLC35F5):c.982G>A (p.Val328Ile)not specified [RCV004167785]likely benign2113731587113731587Humanname
401720448CV2673329single nucleotide variantNM_025181.5(SLC35F5):c.734T>G (p.Phe245Cys)not specified [RCV004288314]uncertain significance2113742708113742708Humanname
401886385CV2771210single nucleotide variantNM_025181.5(SLC35F5):c.805A>G (p.Ile269Val)not specified [RCV004346196]uncertain significance2113735804113735804Humanname
401891723CV2780702single nucleotide variantNM_025181.5(SLC35F5):c.872A>G (p.Asn291Ser)not specified [RCV004352041]uncertain significance2113734634113734634Humanname
405784849CV3332805single nucleotide variantNM_025181.5(SLC35F5):c.370T>C (p.Trp124Arg)not specified [RCV004459323]uncertain significance2113750472113750472Humanname
405784855CV3332806single nucleotide variantNM_025181.5(SLC35F5):c.652A>G (p.Met218Val)not specified [RCV004459324]uncertain significance2113742790113742790Humanname
407510131CV3484469single nucleotide variantNM_025181.5(SLC35F5):c.649C>T (p.Arg217Cys)not specified [RCV004672624]uncertain significance2113742793113742793Humanname
407510138CV3484471single nucleotide variantNM_025181.5(SLC35F5):c.445G>C (p.Ala149Pro)not specified [RCV004672626]uncertain significance2113746312113746312Humanname
407510144CV3484473single nucleotide variantNM_025181.5(SLC35F5):c.569A>G (p.Lys190Arg)not specified [RCV004672628]uncertain significance2113742873113742873Humanname
407510150CV3484475single nucleotide variantNM_025181.5(SLC35F5):c.426T>G (p.Asp142Glu)not specified [RCV004672630]uncertain significance2113746331113746331Humanname
597765808CV3599731single nucleotide variantNM_025181.5(SLC35F5):c.578G>A (p.Arg193His)not specified [RCV004870372]uncertain significance2113742864113742864Humanname
597702565CV3599737single nucleotide variantNM_025181.5(SLC35F5):c.541A>G (p.Thr181Ala)not specified [RCV004860103]uncertain significance2113743734113743734Humanname
598242990CV3914835single nucleotide variantNM_025181.5(SLC35F5):c.668A>C (p.Lys223Thr)not specified [RCV005276628]uncertain significance2113742774113742774Humanname
15098480CV696983single nucleotide variantNM_025181.5(SLC35F5):c.819A>T (p.Leu273Phe)not provided [RCV000958569]likely benign2113735790113735790Humanname
156263839CV2289735single nucleotide variantNM_025181.5(SLC35F5):c.1501C>G (p.Pro501Ala)not specified [RCV004150428]uncertain significance2113717846113717846Humanname
401773147CV2709150single nucleotide variantNM_025181.5(SLC35F5):c.1483C>T (p.His495Tyr)not specified [RCV004316337]uncertain significance2113719167113719167Humanname
401764745CV2728058single nucleotide variantNM_025181.5(SLC35F5):c.1192A>G (p.Met398Val)not specified [RCV004324171]uncertain significance2113725436113725436Humanname
407510135CV3484470single nucleotide variantNM_025181.5(SLC35F5):c.1475G>T (p.Cys492Phe)not specified [RCV004672625]uncertain significance2113719175113719175Humanname
597765805CV3599733single nucleotide variantNM_025181.5(SLC35F5):c.1127C>T (p.Pro376Leu)not specified [RCV004870373]uncertain significance2113725501113725501Humanname