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41 records found for search term Atg16l1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405262515CV3200154single nucleotide variantNM_030803.7(ATG16L1):c.60A>G (p.Gln20=)ATG16L1-related disorder [RCV003967273]likely benign2233251887233251887Humanname , trait , alternate_id
405265167CV3198555single nucleotide variantNM_030803.7(ATG16L1):c.552G>A (p.Thr184=)ATG16L1-related disorder [RCV003897304]likely benign2233265054233265054Humanname , trait , alternate_id
10051589CV193644single nucleotide variantNM_030803.7(ATG16L1):c.220G>A (p.Asp74Asn)not provided [RCV000177298]uncertain significance2233263140233263140Humanname
156145260CV2218765single nucleotide variantNM_030803.7(ATG16L1):c.187G>A (p.Val63Ile)not specified [RCV004085017]likely benign2233256173233256173Humanname
155919270CV2279391single nucleotide variantNM_030803.7(ATG16L1):c.139G>C (p.Asp47His)not specified [RCV004141942]uncertain significance2233256125233256125Humanname
401876313CV2774460single nucleotide variantNM_030803.7(ATG16L1):c.157G>T (p.Ala53Ser)not specified [RCV004347795]uncertain significance2233256143233256143Humanname
405283795CV3200356single nucleotide variantNM_030803.7(ATG16L1):c.1284C>T (p.His428=)ATG16L1-related disorder [RCV003979402]likely benign2233289934233289934Humanname , trait , alternate_id
405273036CV3210321single nucleotide variantNM_030803.7(ATG16L1):c.1779C>T (p.Val593=)ATG16L1-related disorder [RCV003914548]likely benign2233294305233294305Humanname , trait , alternate_id
405688773CV3279785single nucleotide variantNM_030803.7(ATG16L1):c.126G>T (p.Leu42Phe)not specified [RCV004423284]uncertain significance2233256112233256112Humanname
407494906CV3474260single nucleotide variantNM_030803.7(ATG16L1):c.1629C>T (p.Ser543=)not specified [RCV004667747]likely benign2233293256233293256Humanname
598267724CV3911108single nucleotide variantNM_030803.7(ATG16L1):c.152T>C (p.Val51Ala)not specified [RCV005281639]uncertain significance2233256138233256138Humanname
617153109CV4021082single nucleotide variantNM_030803.7(ATG16L1):c.1674G>A (p.Leu558=)not provided [RCV005428835]likely benign2233293301233293301Humanname
15195918CV697414single nucleotide variantNM_030803.7(ATG16L1):c.1788C>T (p.Asp596=)not provided [RCV000956055]benign2233294314233294314Humanname
8555994CV16169single nucleotide variantNM_030803.7(ATG16L1):c.898A>G (p.Thr300Ala)ATG16L1-related disorder [RCV003982820]|Inflammatory bowel disease 10, susceptibility to [RCV000001189]|not provided [RCV004707847]|not specified [RCV000180346]risk factor|benign2233274722233274722Human5name , trait , alternate_id
8555994CV16169single nucleotide variantNM_030803.7(ATG16L1):c.898A>G (p.Thr300Ala)ATG16L1-related disorder [RCV003982820]|Inflammatory bowel disease 10, susceptibility to [RCV000001189]|not provided [RCV004707847]|not specified [RCV000180346]risk factor|benign2233274722233274723Human5name , trait , alternate_id
156180888CV2288129single nucleotide variantNM_030803.7(ATG16L1):c.428C>T (p.Thr143Met)not specified [RCV004149659]uncertain significance2233264930233264930Humanname
156006041CV2394102single nucleotide variantNM_030803.7(ATG16L1):c.514A>G (p.Thr172Ala)not specified [RCV004236309]uncertain significance2233265016233265016Humanname
401740410CV2681403single nucleotide variantNM_030803.7(ATG16L1):c.886G>A (p.Asp296Asn)not specified [RCV004291948]uncertain significance2233274710233274710Humanname
401897007CV2785493single nucleotide variantNM_030803.7(ATG16L1):c.409A>T (p.Thr137Ser)not specified [RCV004363021]uncertain significance2233264911233264911Humanname
405289813CV3218975single nucleotide variantNM_030803.7(ATG16L1):c.656G>A (p.Arg219Gln)ATG16L1-related disorder [RCV003962023]likely benign2233270016233270016Humanname , trait , alternate_id
407452365CV3474268single nucleotide variantNM_030803.7(ATG16L1):c.715G>T (p.Asp239Tyr)not specified [RCV004684012]uncertain significance2233272973233272973Humanname
597623063CV3552421single nucleotide variantNM_030803.7(ATG16L1):c.773G>A (p.Arg258Gln)Inflammatory bowel disease 10 [RCV004821367]uncertain significance2233273031233273031Human1name
597677048CV3596387single nucleotide variantNM_030803.7(ATG16L1):c.442C>G (p.Leu148Val)not specified [RCV004857029]uncertain significance2233264944233264944Humanname
597677057CV3596393single nucleotide variantNM_030803.7(ATG16L1):c.739A>G (p.Thr247Ala)not specified [RCV004857030]uncertain significance2233272997233272997Humanname
597677136CV3596402single nucleotide variantNM_030803.7(ATG16L1):c.782G>A (p.Ser261Asn)not specified [RCV004857038]uncertain significance2233273040233273040Humanname
597677233CV3596412single nucleotide variantNM_030803.7(ATG16L1):c.355C>T (p.Arg119Trp)not specified [RCV004857048]uncertain significance2233264031233264031Humanname
156169961CV2197842single nucleotide variantNM_030803.7(ATG16L1):c.1262C>T (p.Ala421Val)not specified [RCV004077078]uncertain significance2233289912233289912Humanname
155916131CV2281931single nucleotide variantNM_030803.7(ATG16L1):c.1710G>C (p.Lys570Asn)not specified [RCV004138705]uncertain significance2233293337233293337Humanname
156018908CV2301696single nucleotide variantNM_030803.7(ATG16L1):c.1549C>T (p.Leu517Phe)not specified [RCV004156520]uncertain significance2233292246233292246Humanname
155953886CV2303185single nucleotide variantNM_030803.7(ATG16L1):c.1074C>G (p.Phe358Leu)not specified [RCV004156948]uncertain significance2233281118233281118Humanname
156395832CV2325950single nucleotide variantNM_030803.7(ATG16L1):c.1082C>T (p.Ser361Phe)not specified [RCV004174121]uncertain significance2233281126233281126Humanname
329358836CV2425402single nucleotide variantNM_030803.7(ATG16L1):c.1561G>A (p.Ala521Thr)not specified [RCV004251059]uncertain significance2233292258233292258Humanname
329359547CV2451073single nucleotide variantNM_030803.7(ATG16L1):c.1150G>A (p.Ala384Thr)not specified [RCV004269729]uncertain significance2233282700233282700Humanname
329393848CV2472162single nucleotide variantNM_030803.7(ATG16L1):c.1102G>A (p.Gly368Arg)not specified [RCV004283288]uncertain significance2233281146233281146Humanname
401894671CV2785159single nucleotide variantNM_030803.7(ATG16L1):c.1600G>A (p.Gly534Ser)not specified [RCV004355156]uncertain significance2233292406233292406Humanname
401865900CV2786192single nucleotide variantNM_030803.7(ATG16L1):c.1547A>G (p.Asp516Gly)not specified [RCV004359991]uncertain significance2233292244233292244Humanname
405688778CV3279786single nucleotide variantNM_030803.7(ATG16L1):c.1564A>G (p.Ile522Val)not specified [RCV004423285]likely benign2233292261233292261Humanname
405688781CV3279787single nucleotide variantNM_030803.7(ATG16L1):c.1640G>A (p.Ser547Asn)not specified [RCV004423286]uncertain significance2233293267233293267Humanname
405688786CV3279788single nucleotide variantNM_030803.7(ATG16L1):c.1751C>T (p.Ala584Val)not specified [RCV004423287]uncertain significance2233294277233294277Humanname
405688791CV3279789single nucleotide variantNM_030803.7(ATG16L1):c.1759C>T (p.Pro587Ser)not specified [RCV004423288]uncertain significance2233294285233294285Humanname
405691353CV3227525deletionNM_030803.7(ATG16L1):c.632_633del (p.Lys211fs)Inflammatory bowel disease 10 [RCV003991870]uncertain significance2233265131233265132Human1name