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41 records found for search term Vps37c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597804265CV3626561single nucleotide variantNM_017966.5(VPS37C):c.8C>T (p.Thr3Met)not specified [RCV004882164]uncertain significance116113882261138822Humanname
156014650CV2301525single nucleotide variantNM_017966.5(VPS37C):c.16G>T (p.Asp6Tyr)not specified [RCV004162440]uncertain significance116113881461138814Humanname
598217555CV3925992single nucleotide variantNM_017966.5(VPS37C):c.21G>T (p.Lys7Asn)not specified [RCV005293051]uncertain significance116113880961138809Humanname
156345337CV2372905single nucleotide variantNM_017966.5(VPS37C):c.68A>G (p.Asp23Gly)not specified [RCV004223950]uncertain significance116113876261138762Humanname
405811542CV3342125single nucleotide variantNM_017966.5(VPS37C):c.94G>A (p.Val32Ile)not specified [RCV004482838]uncertain significance116113420761134207Humanname
156402466CV2361481single nucleotide variantNM_017966.5(VPS37C):c.232G>A (p.Val78Met)not specified [RCV004221120]uncertain significance116113406961134069Humanname
405811533CV3342120single nucleotide variantNM_017966.5(VPS37C):c.115C>T (p.Arg39Trp)not specified [RCV004482833]uncertain significance116113418661134186Humanname
405811535CV3342121single nucleotide variantNM_017966.5(VPS37C):c.238C>T (p.Arg80Trp)not specified [RCV004482834]uncertain significance116113406361134063Humanname
597698982CV3626558single nucleotide variantNM_017966.5(VPS37C):c.239G>A (p.Arg80Gln)not specified [RCV004885466]uncertain significance116113406261134062Humanname
598255491CV3925989single nucleotide variantNM_017966.5(VPS37C):c.205G>A (p.Asp69Asn)not specified [RCV005299432]uncertain significance116113409661134096Humanname
598217541CV3925990single nucleotide variantNM_017966.5(VPS37C):c.206A>C (p.Asp69Ala)not specified [RCV005293049]uncertain significance116113409561134095Humanname
156042689CV2215790single nucleotide variantNM_017966.5(VPS37C):c.520C>T (p.Arg174Cys)not specified [RCV004096917]uncertain significance116113236861132368Humanname
156332161CV2220637single nucleotide variantNM_017966.5(VPS37C):c.502G>A (p.Gly168Ser)not specified [RCV004097818]uncertain significance116113238661132386Humanname
156283267CV2230905single nucleotide variantNM_017966.5(VPS37C):c.315G>C (p.Gln105His)not specified [RCV004092377]uncertain significance116113328861133288Humanname
156311163CV2260135single nucleotide variantNM_017966.5(VPS37C):c.632C>T (p.Pro211Leu)not specified [RCV004119131]uncertain significance116113225661132256Humanname
156151981CV2265873single nucleotide variantNM_017966.5(VPS37C):c.448G>A (p.Val150Met)not specified [RCV004126733]uncertain significance116113244061132440Humanname
156261201CV2287476single nucleotide variantNM_017966.5(VPS37C):c.395T>C (p.Phe132Ser)not specified [RCV004140944]uncertain significance116113249361132493Humanname
156273956CV2293720single nucleotide variantNM_017966.5(VPS37C):c.938T>C (p.Ile313Thr)not specified [RCV004155007]likely benign116113195061131950Humanname
156281356CV2295108single nucleotide variantNM_017966.5(VPS37C):c.698A>C (p.Gln233Pro)not specified [RCV004156212]uncertain significance116113219061132190Humanname
156303445CV2308335single nucleotide variantNM_017966.5(VPS37C):c.940C>A (p.Gln314Lys)not specified [RCV004164821]uncertain significance116113194861131948Humanname
156347505CV2315312single nucleotide variantNM_017966.5(VPS37C):c.535G>A (p.Val179Met)not specified [RCV004167296]uncertain significance116113235361132353Humanname
156148737CV2321774single nucleotide variantNM_017966.5(VPS37C):c.776C>G (p.Ser259Cys)not specified [RCV004179766]uncertain significance116113211261132112Humanname
156168072CV2337266single nucleotide variantNM_017966.5(VPS37C):c.907C>G (p.Pro303Ala)not specified [RCV004185720]uncertain significance116113198161131981Humanname
329351546CV2462095single nucleotide variantNM_017966.5(VPS37C):c.333C>G (p.Ile111Met)not specified [RCV004266124]uncertain significance116113327061133270Humanname
401769858CV2718919single nucleotide variantNM_017966.5(VPS37C):c.575A>G (p.Glu192Gly)not specified [RCV004322519]uncertain significance116113231361132313Humanname
401857938CV2763079single nucleotide variantNM_017966.5(VPS37C):c.679C>T (p.Pro227Ser)not specified [RCV004336129]uncertain significance116113220961132209Humanname
405811537CV3342122single nucleotide variantNM_017966.5(VPS37C):c.436C>T (p.Arg146Cys)not specified [RCV004482835]uncertain significance116113245261132452Humanname
405811539CV3342123single nucleotide variantNM_017966.5(VPS37C):c.581C>T (p.Pro194Leu)not specified [RCV004482836]uncertain significance116113230761132307Humanname
405811541CV3342124single nucleotide variantNM_017966.5(VPS37C):c.829A>G (p.Met277Val)not specified [RCV004482837]uncertain significance116113205961132059Humanname
597804263CV3626559single nucleotide variantNM_017966.5(VPS37C):c.767C>T (p.Ala256Val)not specified [RCV004882163]uncertain significance116113212161132121Humanname
597698992CV3626560single nucleotide variantNM_017966.5(VPS37C):c.472A>G (p.Arg158Gly)not specified [RCV004885467]uncertain significance116113241661132416Humanname
597698999CV3626563single nucleotide variantNM_017966.5(VPS37C):c.653C>A (p.Thr218Asn)not specified [RCV004885468]uncertain significance116113223561132235Humanname
597804269CV3626564single nucleotide variantNM_017966.5(VPS37C):c.869G>C (p.Arg290Thr)not specified [RCV004882166]uncertain significance116113201961132019Humanname
597804270CV3626565single nucleotide variantNM_017966.5(VPS37C):c.524C>T (p.Pro175Leu)not specified [RCV004882167]uncertain significance116113236461132364Humanname
597699008CV3626566single nucleotide variantNM_017966.5(VPS37C):c.610C>T (p.Pro204Ser)not specified [RCV004885469]uncertain significance116113227861132278Humanname
597804272CV3626567single nucleotide variantNM_017966.5(VPS37C):c.556A>C (p.Thr186Pro)not specified [RCV004882168]uncertain significance116113233261132332Humanname
598217535CV3925988single nucleotide variantNM_017966.5(VPS37C):c.967C>A (p.Gln323Lys)not specified [RCV005293048]uncertain significance116113192161131921Humanname
598217548CV3925991single nucleotide variantNM_017966.5(VPS37C):c.653C>G (p.Thr218Ser)not specified [RCV005293050]uncertain significance116113223561132235Humanname
407532594CV3491417single nucleotide variantNM_017966.5(VPS37C):c.1016C>T (p.Ala339Val)not specified [RCV004683239]uncertain significance116113187261131872Humanname
597804267CV3626562single nucleotide variantNM_017966.5(VPS37C):c.1015G>A (p.Ala339Thr)not specified [RCV004882165]uncertain significance116113187361131873Humanname
598217529CV3925987single nucleotide variantNM_017966.5(VPS37C):c.1043C>T (p.Pro348Leu)not specified [RCV005293047]uncertain significance116113184561131845Humanname