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69 records found for search term Galnt10
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
40814938CV970175single nucleotide variantNM_198321.4(GALNT10):c.263-139G>Cnot provided [RCV004706079]|not specified [RCV001261640]benign|likely benign5154297802154297802Humanname
40814940CV970176single nucleotide variantNM_198321.4(GALNT10):c.263-138A>Tnot provided [RCV004706080]|not specified [RCV001261641]benign|likely benign5154297803154297803Humanname
8580451CV114881single nucleotide variantNM_198321.3(GALNT10):c.569-10665C>GLung cancer [RCV000095404]uncertain significance5154365612154365612Humanname
407486920CV3436205single nucleotide variantNM_198321.4(GALNT10):c.20G>A (p.Arg7Gln)not specified [RCV004619178]uncertain significance5154190886154190886Humanname
407486914CV3436204single nucleotide variantNM_198321.4(GALNT10):c.71A>G (p.Asn24Ser)not specified [RCV004619177]uncertain significance5154190937154190937Humanname
597753694CV3673549single nucleotide variantNM_198321.4(GALNT10):c.89T>C (p.Leu30Pro)not specified [RCV004924196]uncertain significance5154190955154190955Humanname
8625967CV81111single nucleotide variantNM_198321.3(GALNT10):c.312G>A (p.Val104=)Malignant melanoma [RCV000061189]not provided5154297990154297990Humanname
8625968CV81112single nucleotide variantNM_198321.3(GALNT10):c.549C>T (p.Val183=)Malignant melanoma [RCV000061190]not provided5154329719154329719Humanname
8631499CV86703single nucleotide variantNM_198321.3(GALNT10):c.495C>T (p.Val165=)Malignant melanoma [RCV000066794]not provided5154329665154329665Humanname
156113153CV2212666single nucleotide variantNM_198321.4(GALNT10):c.134C>G (p.Ala45Gly)not specified [RCV004085183]uncertain significance5154191000154191000Humanname
156223753CV2395018single nucleotide variantNM_198321.4(GALNT10):c.256C>T (p.Arg86Cys)not specified [RCV004236709]uncertain significance5154294912154294912Humanname
405255956CV3208436single nucleotide variantNM_198321.4(GALNT10):c.1356C>T (p.Pro452=)GALNT10-related disorder [RCV003939534]likely benign5154409732154409732Humanname , trait , alternate_id
405748868CV3254351single nucleotide variantNM_198321.4(GALNT10):c.163T>A (p.Ser55Thr)not specified [RCV004392430]uncertain significance5154294819154294819Humanname
407486887CV3436200single nucleotide variantNM_198321.4(GALNT10):c.143C>A (p.Ala48Glu)not specified [RCV004619173]uncertain significance5154191009154191009Humanname
597753668CV3673542single nucleotide variantNM_198321.4(GALNT10):c.154G>C (p.Gly52Arg)not specified [RCV004924190]uncertain significance5154191020154191020Humanname
597753680CV3673546single nucleotide variantNM_198321.4(GALNT10):c.296C>T (p.Thr99Ile)not specified [RCV004924193]uncertain significance5154297974154297974Humanname
598202649CV3977596single nucleotide variantNM_198321.4(GALNT10):c.155G>C (p.Gly52Ala)not specified [RCV005337136]uncertain significance5154191021154191021Humanname
598202657CV3977597single nucleotide variantNM_198321.4(GALNT10):c.221G>C (p.Trp74Ser)not specified [RCV005337137]uncertain significance5154294877154294877Humanname
598202666CV3977598single nucleotide variantNM_198321.4(GALNT10):c.185C>G (p.Thr62Arg)not specified [RCV005337138]uncertain significance5154294841154294841Humanname
15196959CV698980single nucleotide variantNM_198321.4(GALNT10):c.1626G>A (p.Lys542=)not provided [RCV000956332]benign5154415905154415905Humanname
156399460CV2205133single nucleotide variantNM_198321.4(GALNT10):c.806T>C (p.Ile269Thr)not specified [RCV004077731]uncertain significance5154380499154380499Humanname
156065439CV2225329single nucleotide variantNM_198321.4(GALNT10):c.488G>T (p.Arg163Leu)not specified [RCV004100754]uncertain significance5154329658154329658Humanname
155944825CV2237876single nucleotide variantNM_198321.4(GALNT10):c.493G>A (p.Val165Ile)not specified [RCV004109104]uncertain significance5154329663154329663Humanname
156368834CV2267095single nucleotide variantNM_198321.4(GALNT10):c.640C>T (p.Arg214Trp)not specified [RCV004131718]uncertain significance5154376348154376348Humanname
156129689CV2279710single nucleotide variantNM_198321.4(GALNT10):c.523G>C (p.Glu175Gln)not specified [RCV004144329]uncertain significance5154329693154329693Humanname
155924159CV2280479single nucleotide variantNM_198321.4(GALNT10):c.604C>T (p.Leu202Phe)not specified [RCV004140642]uncertain significance5154376312154376312Humanname
156146575CV2289237single nucleotide variantNM_198321.4(GALNT10):c.529G>C (p.Val177Leu)not specified [RCV004152228]uncertain significance5154329699154329699Humanname
156363149CV2330553single nucleotide variantNM_198321.4(GALNT10):c.509A>G (p.Asn170Ser)not specified [RCV004181116]uncertain significance5154329679154329679Humanname
156134972CV2362148single nucleotide variantNM_198321.4(GALNT10):c.854G>A (p.Arg285Gln)not specified [RCV004209951]uncertain significance5154380547154380547Humanname
155992673CV2381564single nucleotide variantNM_198321.4(GALNT10):c.598A>G (p.Met200Val)not specified [RCV004230034]uncertain significance5154376306154376306Humanname
156390984CV2384992single nucleotide variantNM_198321.4(GALNT10):c.682G>T (p.Ala228Ser)not specified [RCV004228264]uncertain significance5154376390154376390Humanname
329379275CV2456183single nucleotide variantNM_198321.4(GALNT10):c.551A>C (p.Asp184Ala)not specified [RCV004273372]uncertain significance5154329721154329721Humanname
401739452CV2673289single nucleotide variantNM_198321.4(GALNT10):c.415C>T (p.Arg139Cys)not specified [RCV004286089]uncertain significance5154329585154329585Humanname
401897350CV2790048single nucleotide variantNM_198321.4(GALNT10):c.823C>T (p.Arg275Trp)not specified [RCV004364000]uncertain significance5154380516154380516Humanname
405748883CV3254353single nucleotide variantNM_198321.4(GALNT10):c.886C>T (p.Arg296Trp)not specified [RCV004392432]uncertain significance5154380579154380579Humanname
405748892CV3254354single nucleotide variantNM_198321.4(GALNT10):c.899C>T (p.Pro300Leu)not specified [RCV004392433]uncertain significance5154380592154380592Humanname
597779697CV3673538single nucleotide variantNM_198321.4(GALNT10):c.994C>T (p.Leu332Phe)not specified [RCV004930446]uncertain significance5154386368154386368Humanname
597753659CV3673539single nucleotide variantNM_198321.4(GALNT10):c.893C>T (p.Pro298Leu)not specified [RCV004924188]uncertain significance5154380586154380586Humanname
597779700CV3673540single nucleotide variantNM_198321.4(GALNT10):c.814G>A (p.Asp272Asn)not specified [RCV004930447]uncertain significance5154380507154380507Humanname
597753663CV3673541single nucleotide variantNM_198321.4(GALNT10):c.313G>A (p.Asp105Asn)not specified [RCV004924189]uncertain significance5154297991154297991Humanname
597753672CV3673543single nucleotide variantNM_198321.4(GALNT10):c.838G>T (p.Ala280Ser)not specified [RCV004924191]uncertain significance5154380531154380531Humanname
597753689CV3673548single nucleotide variantNM_198321.4(GALNT10):c.389T>C (p.Ile130Thr)not specified [RCV004924195]uncertain significance5154298067154298067Humanname
598202642CV3977595single nucleotide variantNM_198321.4(GALNT10):c.349G>A (p.Val117Ile)not specified [RCV005337135]uncertain significance5154298027154298027Humanname
598202673CV3977599single nucleotide variantNM_198321.4(GALNT10):c.873G>C (p.Glu291Asp)not specified [RCV005337139]uncertain significance5154380566154380566Humanname
156242280CV2210641single nucleotide variantNM_198321.4(GALNT10):c.1535G>A (p.Arg512Gln)not specified [RCV004083786]uncertain significance5154415814154415814Humanname
156231354CV2264382single nucleotide variantNM_198321.4(GALNT10):c.1469G>C (p.Arg490Pro)not specified [RCV004138286]uncertain significance5154412971154412971Humanname
156266596CV2275484single nucleotide variantNM_198321.4(GALNT10):c.1802A>G (p.Asn601Ser)not specified [RCV004137139]uncertain significance5154416962154416962Humanname
156281137CV2338440single nucleotide variantNM_198321.4(GALNT10):c.1357G>A (p.Val453Met)not specified [RCV004186483]uncertain significance5154409733154409733Humanname
156004094CV2396865single nucleotide variantNM_198321.4(GALNT10):c.1774A>G (p.Thr592Ala)not specified [RCV004233991]uncertain significance5154416934154416934Humanname
329358759CV2450692single nucleotide variantNM_198321.4(GALNT10):c.1669C>T (p.His557Tyr)not specified [RCV004267642]uncertain significance5154416829154416829Humanname
401723487CV2724919single nucleotide variantNM_198321.4(GALNT10):c.1475G>A (p.Arg492His)not specified [RCV004319687]uncertain significance5154412977154412977Humanname
401886197CV2774889single nucleotide variantNM_198321.4(GALNT10):c.1576G>A (p.Ala526Thr)not specified [RCV004343968]uncertain significance5154415855154415855Humanname
405748864CV3254350single nucleotide variantNM_198321.4(GALNT10):c.1076G>A (p.Arg359His)not specified [RCV004392429]uncertain significance5154404123154404123Humanname
405748875CV3254352single nucleotide variantNM_198321.4(GALNT10):c.1753C>G (p.Gln585Glu)not specified [RCV004392431]uncertain significance5154416913154416913Humanname
407486727CV3436196single nucleotide variantNM_198321.4(GALNT10):c.1601C>T (p.Thr534Met)not specified [RCV004619169]uncertain significance5154415880154415880Humanname
407486870CV3436197single nucleotide variantNM_198321.4(GALNT10):c.1204G>A (p.Ala402Thr)not specified [RCV004619170]uncertain significance5154409580154409580Humanname
407486876CV3436198single nucleotide variantNM_198321.4(GALNT10):c.1465G>A (p.Val489Ile)not specified [RCV004619171]likely benign5154412967154412967Humanname
407486896CV3436201single nucleotide variantNM_198321.4(GALNT10):c.1793A>G (p.Glu598Gly)not specified [RCV004619174]uncertain significance5154416953154416953Humanname
407486903CV3436202single nucleotide variantNM_198321.4(GALNT10):c.1649G>T (p.Arg550Leu)not specified [RCV004619175]uncertain significance5154415928154415928Humanname
407486909CV3436203single nucleotide variantNM_198321.4(GALNT10):c.1636C>A (p.Leu546Met)not specified [RCV004619176]uncertain significance5154415915154415915Humanname
408384333CV3505092single nucleotide variantNM_198321.4(GALNT10):c.1201T>G (p.Tyr401Asp)GALNT10-related disorder [RCV004731723]uncertain significance5154409577154409577Humanname , trait , alternate_id
597753644CV3673533single nucleotide variantNM_198321.4(GALNT10):c.1048T>G (p.Ser350Ala)not specified [RCV004924184]uncertain significance5154386422154386422Humanname
597753651CV3673535single nucleotide variantNM_198321.4(GALNT10):c.1469G>A (p.Arg490Gln)not specified [RCV004924186]uncertain significance5154412971154412971Humanname
597779694CV3673536single nucleotide variantNM_198321.4(GALNT10):c.1223G>A (p.Arg408His)not specified [RCV004930445]uncertain significance5154409599154409599Humanname
597753655CV3673537single nucleotide variantNM_198321.4(GALNT10):c.1421C>T (p.Thr474Ile)not specified [RCV004924187]uncertain significance5154412923154412923Humanname
597753676CV3673545single nucleotide variantNM_198321.4(GALNT10):c.1620C>A (p.Ser540Arg)not specified [RCV004924192]uncertain significance5154415899154415899Humanname
597753684CV3673547single nucleotide variantNM_198321.4(GALNT10):c.1343A>G (p.Lys448Arg)not specified [RCV004924194]uncertain significance5154409719154409719Humanname
15121066CV734984single nucleotide variantNM_198321.4(GALNT10):c.1391G>A (p.Arg464Gln)not provided [RCV000895997]likely benign5154412893154412893Humanname
8631500CV86704single nucleotide variantNM_198321.3(GALNT10):c.1231G>A (p.Glu411Lys)Malignant melanoma [RCV000066795]not provided5154409607154409607Humanname