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Variants search result for Homo sapiens
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63 records found for search term Slc46a2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8650983CV127558single nucleotide variantNM_033051.3(SLC46A2):c.-1563C>GLung cancer [RCV000108045]uncertain significance9112892244112892244Humanname
8650982CV127557single nucleotide variantNM_033051.3(SLC46A2):c.1129+3G>ALung cancer [RCV000108044]uncertain significance9112889550112889550Humanname
597766541CV3596737single nucleotide variantNM_033051.4(SLC46A2):c.20G>A (p.Cys7Tyr)not specified [RCV004870638]uncertain significance9112890662112890662Humanname
155937402CV2373576single nucleotide variantNM_033051.4(SLC46A2):c.73G>A (p.Val25Met)not specified [RCV004222673]uncertain significance9112890609112890609Humanname
405711175CV3329420single nucleotide variantNM_033051.4(SLC46A2):c.97G>A (p.Ala33Thr)not specified [RCV004461809]uncertain significance9112890585112890585Humanname
598244878CV3911278single nucleotide variantNM_033051.4(SLC46A2):c.31G>T (p.Gly11Cys)not specified [RCV005276914]uncertain significance9112890651112890651Humanname
15104514CV700736single nucleotide variantNM_033051.4(SLC46A2):c.777T>C (p.Asp259=)not provided [RCV000959702]benign9112889905112889905Humanname
15156512CV723251single nucleotide variantNM_033051.4(SLC46A2):c.759C>T (p.Tyr253=)not provided [RCV000880643]benign9112889923112889923Humanname
15160182CV723252single nucleotide variantNM_033051.4(SLC46A2):c.726C>T (p.Ala242=)not provided [RCV000881333]benign9112889956112889956Humanname
156240769CV2265595single nucleotide variantNM_033051.4(SLC46A2):c.115G>A (p.Gly39Arg)not specified [RCV004124330]uncertain significance9112890567112890567Humanname
156166521CV2319945single nucleotide variantNM_033051.4(SLC46A2):c.218C>T (p.Ala73Val)not specified [RCV004167822]uncertain significance9112890464112890464Humanname
156247036CV2357025single nucleotide variantNM_033051.4(SLC46A2):c.284G>A (p.Gly95Glu)not specified [RCV004206830]uncertain significance9112890398112890398Humanname
156188150CV2375292single nucleotide variantNM_033051.4(SLC46A2):c.250G>A (p.Val84Met)not specified [RCV004232702]uncertain significance9112890432112890432Humanname
405711112CV3329410single nucleotide variantNM_033051.4(SLC46A2):c.112G>A (p.Ala38Thr)not specified [RCV004461799]uncertain significance9112890570112890570Humanname
405711137CV3329414single nucleotide variantNM_033051.4(SLC46A2):c.263C>T (p.Ser88Phe)not specified [RCV004461803]uncertain significance9112890419112890419Humanname
598244819CV3911270single nucleotide variantNM_033051.4(SLC46A2):c.164A>G (p.Asn55Ser)not specified [RCV005276907]uncertain significance9112890518112890518Humanname
598244861CV3911275single nucleotide variantNM_033051.4(SLC46A2):c.109G>C (p.Asp37His)not specified [RCV005276912]uncertain significance9112890573112890573Humanname
156236696CV2206692single nucleotide variantNM_033051.4(SLC46A2):c.338T>C (p.Leu113Pro)not specified [RCV004083386]uncertain significance9112890344112890344Humanname
156202377CV2234491single nucleotide variantNM_033051.4(SLC46A2):c.842C>T (p.Thr281Ile)not specified [RCV004100692]uncertain significance9112889840112889840Humanname
155977645CV2246894single nucleotide variantNM_033051.4(SLC46A2):c.688C>T (p.Pro230Ser)not specified [RCV004112697]uncertain significance9112889994112889994Humanname
156121165CV2275990single nucleotide variantNM_033051.4(SLC46A2):c.635G>C (p.Ser212Thr)not specified [RCV004141670]uncertain significance9112890047112890047Humanname
155956737CV2281961single nucleotide variantNM_033051.4(SLC46A2):c.871A>G (p.Ile291Val)not specified [RCV004138728]uncertain significance9112889811112889811Humanname
155908533CV2302450single nucleotide variantNM_033051.4(SLC46A2):c.907G>T (p.Val303Leu)not specified [RCV004161183]uncertain significance9112889775112889775Humanname
155905299CV2349730single nucleotide variantNM_033051.4(SLC46A2):c.314G>C (p.Arg105Pro)not specified [RCV004204144]uncertain significance9112890368112890368Humanname
156050647CV2378484single nucleotide variantNM_033051.4(SLC46A2):c.389A>G (p.Asp130Gly)not specified [RCV004228540]uncertain significance9112890293112890293Humanname
155936494CV2380475single nucleotide variantNM_033051.4(SLC46A2):c.761G>A (p.Arg254His)not specified [RCV004218070]uncertain significance9112889921112889921Humanname
329393826CV2472150single nucleotide variantNM_033051.4(SLC46A2):c.488G>C (p.Gly163Ala)not specified [RCV004283276]uncertain significance9112890194112890194Humanname
401760838CV2706116single nucleotide variantNM_033051.4(SLC46A2):c.904G>A (p.Asp302Asn)not specified [RCV004314805]uncertain significance9112889778112889778Humanname
401761311CV2726712single nucleotide variantNM_033051.4(SLC46A2):c.311A>C (p.His104Pro)not specified [RCV004323045]uncertain significance9112890371112890371Humanname
401877686CV2761263single nucleotide variantNM_033051.4(SLC46A2):c.314G>A (p.Arg105Gln)not specified [RCV004341137]uncertain significance9112890368112890368Humanname
405711144CV3329415single nucleotide variantNM_033051.4(SLC46A2):c.515G>A (p.Arg172His)not specified [RCV004461804]uncertain significance9112890167112890167Humanname
405711157CV3329417single nucleotide variantNM_033051.4(SLC46A2):c.643T>A (p.Cys215Ser)not specified [RCV004461806]uncertain significance9112890039112890039Humanname
405711163CV3329418single nucleotide variantNM_033051.4(SLC46A2):c.794A>G (p.Tyr265Cys)not specified [RCV004461807]likely benign9112889888112889888Humanname
405711169CV3329419single nucleotide variantNM_033051.4(SLC46A2):c.907G>A (p.Val303Met)not specified [RCV004461808]uncertain significance9112889775112889775Humanname
407452031CV3484736single nucleotide variantNM_033051.4(SLC46A2):c.734C>A (p.Thr245Asn)not specified [RCV004683779]uncertain significance9112889948112889948Humanname
597723688CV3596731single nucleotide variantNM_033051.4(SLC46A2):c.899C>T (p.Thr300Ile)not specified [RCV004862256]uncertain significance9112889783112889783Humanname
597766520CV3596732single nucleotide variantNM_033051.4(SLC46A2):c.736G>A (p.Val246Met)not specified [RCV004870634]uncertain significance9112889946112889946Humanname
597766525CV3596733single nucleotide variantNM_033051.4(SLC46A2):c.746C>T (p.Thr249Met)not specified [RCV004870635]uncertain significance9112889936112889936Humanname
597766531CV3596734single nucleotide variantNM_033051.4(SLC46A2):c.471G>A (p.Met157Ile)not specified [RCV004870636]uncertain significance9112890211112890211Humanname
597766537CV3596736single nucleotide variantNM_033051.4(SLC46A2):c.694T>C (p.Ser232Pro)not specified [RCV004870637]uncertain significance9112889988112889988Humanname
597723710CV3596738single nucleotide variantNM_033051.4(SLC46A2):c.520A>G (p.Ile174Val)not specified [RCV004862258]uncertain significance9112890162112890162Humanname
598237380CV3911269single nucleotide variantNM_033051.4(SLC46A2):c.685G>A (p.Val229Ile)not specified [RCV005275644]uncertain significance9112889997112889997Humanname
598244827CV3911271single nucleotide variantNM_033051.4(SLC46A2):c.505C>T (p.Arg169Cys)not specified [RCV005276908]uncertain significance9112890177112890177Humanname
598244836CV3911272single nucleotide variantNM_033051.4(SLC46A2):c.890T>C (p.Val297Ala)not specified [RCV005276909]uncertain significance9112889792112889792Humanname
598244843CV3911273single nucleotide variantNM_033051.4(SLC46A2):c.569C>T (p.Ala190Val)not specified [RCV005276910]uncertain significance9112890113112890113Humanname
598237385CV3911276single nucleotide variantNM_033051.4(SLC46A2):c.821G>C (p.Gly274Ala)not specified [RCV005275645]uncertain significance9112889861112889861Humanname
598244870CV3911277single nucleotide variantNM_033051.4(SLC46A2):c.424C>G (p.Leu142Val)not specified [RCV005276913]uncertain significance9112890258112890258Humanname
598244887CV3911279single nucleotide variantNM_033051.4(SLC46A2):c.547G>C (p.Ala183Pro)not specified [RCV005276915]uncertain significance9112890135112890135Humanname
156284960CV2317593single nucleotide variantNM_033051.4(SLC46A2):c.1357A>G (p.Ile453Val)not specified [RCV004172539]uncertain significance9112886473112886473Humanname
329375412CV2440126single nucleotide variantNM_033051.4(SLC46A2):c.1076G>A (p.Gly359Glu)not specified [RCV004260589]uncertain significance9112889606112889606Humanname
329363840CV2469418single nucleotide variantNM_033051.4(SLC46A2):c.1016T>C (p.Leu339Pro)not specified [RCV004282881]uncertain significance9112889666112889666Humanname
401877649CV2761245single nucleotide variantNM_033051.4(SLC46A2):c.1415T>C (p.Ile472Thr)not specified [RCV004341122]uncertain significance9112879775112879775Humanname
401888355CV2788375single nucleotide variantNM_033051.4(SLC46A2):c.1331T>C (p.Leu444Pro)not specified [RCV004352947]uncertain significance9112886499112886499Humanname
405711098CV3329408single nucleotide variantNM_033051.4(SLC46A2):c.1012G>A (p.Val338Ile)not specified [RCV004461797]uncertain significance9112889670112889670Humanname
405711105CV3329409single nucleotide variantNM_033051.4(SLC46A2):c.1037G>A (p.Arg346Gln)not specified [RCV004461798]likely benign9112889645112889645Humanname
405711117CV3329411single nucleotide variantNM_033051.4(SLC46A2):c.1205C>G (p.Ser402Cys)not specified [RCV004461800]uncertain significance9112887338112887338Humanname
405711123CV3329412single nucleotide variantNM_033051.4(SLC46A2):c.1225G>A (p.Val409Ile)not specified [RCV004461801]uncertain significance9112886605112886605Humanname
405711130CV3329413single nucleotide variantNM_033051.4(SLC46A2):c.1310T>C (p.Phe437Ser)not specified [RCV004461802]uncertain significance9112886520112886520Humanname
407515048CV3484735single nucleotide variantNM_033051.4(SLC46A2):c.1106A>G (p.Lys369Arg)not specified [RCV004674789]uncertain significance9112889576112889576Humanname
597723699CV3596735single nucleotide variantNM_033051.4(SLC46A2):c.1127T>C (p.Ile376Thr)not specified [RCV004862257]uncertain significance9112889555112889555Humanname
597766547CV3596739single nucleotide variantNM_033051.4(SLC46A2):c.1402C>T (p.Pro468Ser)not specified [RCV004870639]uncertain significance9112879788112879788Humanname
598244852CV3911274single nucleotide variantNM_033051.4(SLC46A2):c.1133G>A (p.Arg378Gln)not specified [RCV005276911]uncertain significance9112887410112887410Humanname
15157757CV723250single nucleotide variantNM_033051.4(SLC46A2):c.1097C>T (p.Ala366Val)not provided [RCV000880878]benign9112889585112889585Humanname