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Variants search result for Homo sapiens
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42 records found for search term Galnt4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401894297CV2780625single nucleotide variantNM_003774.5(GALNT4):c.19T>C (p.Trp7Arg)not specified [RCV004351982]uncertain significance128952453189524531Humanname
329393135CV2449514single nucleotide variantNM_003774.5(GALNT4):c.50T>G (p.Phe17Cys)not specified [RCV004268452]uncertain significance128952450089524500Humanname
401909890CV2816752single nucleotide variantNM_003774.5(GALNT4):c.978G>A (p.Thr326=)not provided [RCV003398213]likely benign128952357289523572Humanname
407479126CV3436304single nucleotide variantNM_003774.5(GALNT4):c.41T>C (p.Leu14Pro)not specified [RCV004623777]uncertain significance128952450989524509Humanname
10448559CV204620single nucleotide variantNM_003774.5(GALNT4):c.1194C>T (p.Asn398=)Childhood-onset schizophrenia [RCV000202342]likely pathogenic128952335689523356Human1name
401743096CV2684014single nucleotide variantNM_003774.5(GALNT4):c.106G>T (p.Ala36Ser)not specified [RCV004295619]uncertain significance128952444489524444Humanname
405749721CV3254472single nucleotide variantNM_003774.5(GALNT4):c.118C>A (p.Arg40Ser)not specified [RCV004392552]uncertain significance128952443289524432Humanname
405749728CV3254473single nucleotide variantNM_003774.5(GALNT4):c.122C>T (p.Ala41Val)not specified [RCV004392553]uncertain significance128952442889524428Humanname
405749736CV3254474single nucleotide variantNM_003774.5(GALNT4):c.124A>G (p.Arg42Gly)not specified [RCV004392554]uncertain significance128952442689524426Humanname
405749744CV3254475single nucleotide variantNM_003774.5(GALNT4):c.126G>T (p.Arg42Ser)not specified [RCV004392555]uncertain significance128952442489524424Humanname
405749827CV3254487single nucleotide variantNM_003774.5(GALNT4):c.296G>T (p.Arg99Ile)not specified [RCV004392567]uncertain significance128952425489524254Humanname
405749833CV3254488single nucleotide variantNM_003774.5(GALNT4):c.353A>T (p.Asp118Val)not specified [RCV004392568]uncertain significance128952419789524197Humanname
405749841CV3254489single nucleotide variantNM_003774.5(GALNT4):c.359G>C (p.Arg120Thr)not specified [RCV004392569]uncertain significance128952419189524191Humanname
405749848CV3254490single nucleotide variantNM_003774.5(GALNT4):c.380A>G (p.Gln127Arg)not specified [RCV004392570]uncertain significance128952417089524170Humanname
405749853CV3254491single nucleotide variantNM_003774.5(GALNT4):c.422T>C (p.Ile141Thr)not specified [RCV004392571]uncertain significance128952412889524128Humanname
405749860CV3254492single nucleotide variantNM_003774.5(GALNT4):c.435C>G (p.Asn145Lys)not specified [RCV004392572]uncertain significance128952411589524115Humanname
405749867CV3254493single nucleotide variantNM_003774.5(GALNT4):c.529A>T (p.Ser177Cys)not specified [RCV004392573]uncertain significance128952402189524021Humanname
405749872CV3254494single nucleotide variantNM_003774.5(GALNT4):c.586G>C (p.Val196Leu)not specified [RCV004392574]uncertain significance128952396489523964Humanname
405749877CV3254495single nucleotide variantNM_003774.5(GALNT4):c.617G>A (p.Gly206Glu)not specified [RCV004392575]uncertain significance128952393389523933Humanname
405749884CV3254496single nucleotide variantNM_003774.5(GALNT4):c.625A>G (p.Arg209Gly)not specified [RCV004392576]uncertain significance128952392589523925Humanname
405749891CV3254497single nucleotide variantNM_003774.5(GALNT4):c.664G>A (p.Val222Ile)not specified [RCV004392577]uncertain significance128952388689523886Humanname
405749895CV3254498single nucleotide variantNM_003774.5(GALNT4):c.718C>G (p.Leu240Val)not specified [RCV004392578]uncertain significance128952383289523832Humanname
405749902CV3254499single nucleotide variantNM_003774.5(GALNT4):c.767T>C (p.Ile256Thr)not specified [RCV004392579]uncertain significance128952378389523783Humanname
405749909CV3254500single nucleotide variantNM_003774.5(GALNT4):c.824T>C (p.Ile275Thr)not specified [RCV004392580]uncertain significance128952372689523726Humanname
405749917CV3254501single nucleotide variantNM_003774.5(GALNT4):c.985A>G (p.Thr329Ala)not specified [RCV004392581]uncertain significance128952356589523565Humanname
15199009CV725311single nucleotide variantNM_003774.5(GALNT4):c.786T>A (p.Asn262Lys)not provided [RCV000890516]benign128952376489523764Humanname
401766392CV2725509single nucleotide variantNM_003774.5(GALNT4):c.1184A>G (p.Tyr395Cys)not specified [RCV004320129]uncertain significance128952336689523366Humanname
405749706CV3254470single nucleotide variantNM_003774.5(GALNT4):c.1097A>G (p.Lys366Arg)not specified [RCV004392550]uncertain significance128952345389523453Humanname
405749713CV3254471single nucleotide variantNM_003774.5(GALNT4):c.1100G>A (p.Arg367Gln)not specified [RCV004392551]uncertain significance128952345089523450Humanname
405749750CV3254476single nucleotide variantNM_003774.5(GALNT4):c.1300A>G (p.Asn434Asp)not specified [RCV004392556]uncertain significance128952325089523250Humanname
405749757CV3254477single nucleotide variantNM_003774.5(GALNT4):c.1332G>T (p.Trp444Cys)not specified [RCV004392557]uncertain significance128952321889523218Humanname
405749767CV3254478single nucleotide variantNM_003774.5(GALNT4):c.1344T>G (p.Ile448Met)not specified [RCV004392558]uncertain significance128952320689523206Humanname
405749772CV3254479single nucleotide variantNM_003774.5(GALNT4):c.1348A>G (p.Ser450Gly)not specified [RCV004392559]uncertain significance128952320289523202Humanname
405749782CV3254480single nucleotide variantNM_003774.5(GALNT4):c.1349G>T (p.Ser450Ile)not specified [RCV004392560]uncertain significance128952320189523201Humanname
405749789CV3254481single nucleotide variantNM_003774.5(GALNT4):c.1432C>T (p.His478Tyr)not specified [RCV004392561]uncertain significance128952311889523118Humanname
405749794CV3254482single nucleotide variantNM_003774.5(GALNT4):c.1643T>C (p.Leu548Pro)not specified [RCV004392562]uncertain significance128952290789522907Humanname
405749801CV3254483single nucleotide variantNM_003774.5(GALNT4):c.1655G>A (p.Arg552Gln)not specified [RCV004392563]uncertain significance128952289589522895Humanname
405749808CV3254484single nucleotide variantNM_003774.5(GALNT4):c.1670G>A (p.Arg557Gln)not specified [RCV004392564]uncertain significance128952288089522880Humanname
405749815CV3254485single nucleotide variantNM_003774.5(GALNT4):c.1672C>T (p.Pro558Ser)not specified [RCV004392565]uncertain significance128952287889522878Humanname
405749820CV3254486single nucleotide variantNM_003774.5(GALNT4):c.1697A>G (p.Asp566Gly)not specified [RCV004392566]uncertain significance128952285389522853Humanname
15187032CV702536single nucleotide variantNM_003774.5(GALNT4):c.1546C>A (p.Gln516Lys)not provided [RCV000953466]benign|likely benign128952300489523004Humanname
156041086CV2342100single nucleotide variantNM_001199781.2(POC1B-GALNT4):c.1244G>A (p.Arg415Gln)not specified [RCV004191695]uncertain significance128952329789523297Humanname