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36 records found for search term Slc35e1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156042430CV2310972single nucleotide variantNM_024881.5(SLC35E1):c.10G>T (p.Ala4Ser)not specified [RCV004164003]uncertain significance191657235516572355Humanname
405784521CV3332737single nucleotide variantNM_024881.5(SLC35E1):c.19G>C (p.Gly7Arg)not specified [RCV004459255]uncertain significance191657234616572346Humanname
156249669CV2215578single nucleotide variantNM_024881.5(SLC35E1):c.83C>T (p.Ala28Val)not specified [RCV004089344]uncertain significance191657228216572282Humanname
156070410CV2355998single nucleotide variantNM_024881.5(SLC35E1):c.287A>G (p.His96Arg)not specified [RCV004201375]uncertain significance191657207816572078Humanname
401751389CV2696544single nucleotide variantNM_024881.5(SLC35E1):c.280A>G (p.Ser94Gly)not specified [RCV004312601]likely benign191657208516572085Humanname
401751397CV2696546single nucleotide variantNM_024881.5(SLC35E1):c.295T>C (p.Ser99Pro)not specified [RCV004312603]likely benign191657207016572070Humanname
405784527CV3332738single nucleotide variantNM_024881.5(SLC35E1):c.253G>A (p.Ala85Thr)not specified [RCV004459256]uncertain significance191657211216572112Humanname
598242724CV3914784single nucleotide variantNM_024881.5(SLC35E1):c.161C>A (p.Ala54Asp)not specified [RCV005276583]uncertain significance191657220416572204Humanname
156175290CV2254652single nucleotide variantNM_024881.5(SLC35E1):c.389T>C (p.Ile130Thr)not specified [RCV004115139]uncertain significance191657197616571976Humanname
156267069CV2275523single nucleotide variantNM_024881.5(SLC35E1):c.602T>G (p.Phe201Cys)not specified [RCV004137170]uncertain significance191656806016568060Humanname
155986117CV2282499single nucleotide variantNM_024881.5(SLC35E1):c.877G>A (p.Val293Ile)not specified [RCV004133291]uncertain significance191655527716555277Humanname
156344751CV2294200single nucleotide variantNM_024881.5(SLC35E1):c.712T>A (p.Trp238Arg)not specified [RCV004149560]uncertain significance191656657616566576Humanname
156007891CV2299786single nucleotide variantNM_024881.5(SLC35E1):c.464T>C (p.Ile155Thr)not specified [RCV004148944]uncertain significance191657154016571540Humanname
155956492CV2304043single nucleotide variantNM_024881.5(SLC35E1):c.351C>G (p.Phe117Leu)not specified [RCV004170092]uncertain significance191657201416572014Humanname
156044514CV2340113single nucleotide variantNM_024881.5(SLC35E1):c.884A>G (p.Asn295Ser)not specified [RCV004192354]uncertain significance191655527016555270Humanname
155976469CV2342773single nucleotide variantNM_024881.5(SLC35E1):c.382G>A (p.Val128Ile)not provided [RCV004695598]|not specified [RCV004189816]uncertain significance191657198316571983Humanname
156175544CV2355700single nucleotide variantNM_024881.5(SLC35E1):c.763G>A (p.Val255Ile)not specified [RCV004199062]uncertain significance191655539116555391Humanname
156036963CV2374027single nucleotide variantNM_024881.5(SLC35E1):c.699T>A (p.Phe233Leu)not specified [RCV004227153]uncertain significance191656658916566589Humanname
329396112CV2451890single nucleotide variantNM_024881.5(SLC35E1):c.548A>G (p.Glu183Gly)not specified [RCV004276564]uncertain significance191656811416568114Humanname
329374088CV2452837single nucleotide variantNM_024881.5(SLC35E1):c.955G>A (p.Val319Ile)not specified [RCV004275366]uncertain significance191655519916555199Humanname
597765320CV3599677single nucleotide variantNM_024881.5(SLC35E1):c.341C>T (p.Pro114Leu)not specified [RCV004870342]uncertain significance191657202416572024Humanname
597765324CV3599678single nucleotide variantNM_024881.5(SLC35E1):c.835G>A (p.Ala279Thr)not specified [RCV004870343]uncertain significance191655531916555319Humanname
597765336CV3599681single nucleotide variantNM_024881.5(SLC35E1):c.391T>C (p.Trp131Arg)not specified [RCV004870346]uncertain significance191657197416571974Humanname
597765341CV3599682single nucleotide variantNM_024881.5(SLC35E1):c.410A>C (p.Tyr137Ser)not specified [RCV004870347]uncertain significance191657195516571955Humanname
598242716CV3914783single nucleotide variantNM_024881.5(SLC35E1):c.451C>T (p.Leu151Phe)not specified [RCV005276582]uncertain significance191657155316571553Humanname
598242736CV3914786single nucleotide variantNM_024881.5(SLC35E1):c.805G>A (p.Gly269Ser)not specified [RCV005276585]uncertain significance191655534916555349Humanname
156187640CV2195791single nucleotide variantNM_024881.5(SLC35E1):c.1150C>T (p.Arg384Cys)not specified [RCV004076141]uncertain significance191655376216553762Humanname
155965113CV2206332single nucleotide variantNM_024881.5(SLC35E1):c.1012G>A (p.Asp338Asn)not specified [RCV004078669]uncertain significance191655390016553900Humanname
155915543CV2339150single nucleotide variantNM_024881.5(SLC35E1):c.1132G>A (p.Gly378Arg)not specified [RCV004187190]uncertain significance191655378016553780Humanname
156184775CV2346451single nucleotide variantNM_024881.5(SLC35E1):c.1084C>T (p.Arg362Trp)not specified [RCV004206377]uncertain significance191655382816553828Humanname
401725152CV2697293single nucleotide variantNM_024881.5(SLC35E1):c.1111G>A (p.Gly371Ser)not specified [RCV004304052]uncertain significance191655380116553801Humanname
405784511CV3332735single nucleotide variantNM_024881.5(SLC35E1):c.1105C>T (p.His369Tyr)not specified [RCV004459253]uncertain significance191655380716553807Humanname
405784516CV3332736single nucleotide variantNM_024881.5(SLC35E1):c.1183A>G (p.Ser395Gly)not specified [RCV004459254]uncertain significance191655372916553729Humanname
407510007CV3484437single nucleotide variantNM_024881.5(SLC35E1):c.1131C>G (p.His377Gln)not specified [RCV004672603]uncertain significance191655378116553781Humanname
597765328CV3599679single nucleotide variantNM_024881.5(SLC35E1):c.1030A>G (p.Arg344Gly)not specified [RCV004870344]uncertain significance191655388216553882Humanname
597765332CV3599680single nucleotide variantNM_024881.5(SLC35E1):c.1159A>G (p.Ile387Val)not specified [RCV004870345]uncertain significance191655375316553753Humanname