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Variants search result for Homo sapiens
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36 records found for search term Atp4b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405665920CV3286941single nucleotide variantNM_000705.4(ATP4B):c.5C>T (p.Ala2Val)not specified [RCV004418505]uncertain significance13113658140113658140Humanname
155995439CV2259064single nucleotide variantNM_000705.4(ATP4B):c.77C>T (p.Thr26Met)not specified [RCV004120327]uncertain significance13113658068113658068Humanname
156075337CV2291403single nucleotide variantNM_000705.4(ATP4B):c.37C>A (p.Arg13Ser)not specified [RCV004155742]uncertain significance13113658108113658108Humanname
407527674CV3488820single nucleotide variantNM_000705.4(ATP4B):c.50T>C (p.Phe17Ser)not specified [RCV004680096]uncertain significance13113658095113658095Humanname
156166924CV2200967single nucleotide variantNM_000705.4(ATP4B):c.220C>G (p.Gln74Glu)not specified [RCV004074737]uncertain significance13113654835113654835Humanname
155953400CV2303025single nucleotide variantNM_000705.4(ATP4B):c.178T>C (p.Tyr60His)not specified [RCV004156817]uncertain significance13113654877113654877Humanname
401887818CV2768780single nucleotide variantNM_000705.4(ATP4B):c.139T>C (p.Phe47Leu)not specified [RCV004346917]uncertain significance13113654916113654916Humanname
405665905CV3286938single nucleotide variantNM_000705.4(ATP4B):c.179A>G (p.Tyr60Cys)not specified [RCV004418502]uncertain significance13113654876113654876Humanname
405665909CV3286939single nucleotide variantNM_000705.4(ATP4B):c.232C>T (p.Arg78Trp)not specified [RCV004418503]uncertain significance13113654823113654823Humanname
407527669CV3488818single nucleotide variantNM_000705.4(ATP4B):c.248C>A (p.Thr83Asn)not specified [RCV004680094]uncertain significance13113653428113653428Humanname
155923704CV2217699single nucleotide variantNM_000705.4(ATP4B):c.604G>A (p.Ala202Thr)not specified [RCV004083887]likely benign13113651679113651679Humanname
156062088CV2263185single nucleotide variantNM_000705.4(ATP4B):c.808G>A (p.Val270Met)not specified [RCV004131417]uncertain significance13113649442113649442Humanname
156307445CV2331984single nucleotide variantNM_000705.4(ATP4B):c.662C>G (p.Pro221Arg)not specified [RCV004189043]uncertain significance13113650458113650458Humanname
156224734CV2352605single nucleotide variantNM_000705.4(ATP4B):c.778G>A (p.Ala260Thr)not specified [RCV004198639]uncertain significance13113649472113649472Humanname
156172452CV2380822single nucleotide variantNM_000705.4(ATP4B):c.865A>T (p.Ile289Phe)not specified [RCV004218381]uncertain significance13113649385113649385Humanname
329384558CV2435134single nucleotide variantNM_000705.4(ATP4B):c.464C>T (p.Thr155Met)not specified [RCV004252775]uncertain significance13113652964113652964Humanname
329365093CV2440032single nucleotide variantNM_000705.4(ATP4B):c.638C>T (p.Pro213Leu)not specified [RCV004260506]uncertain significance13113650482113650482Humanname
401753609CV2684999single nucleotide variantNM_000705.4(ATP4B):c.623G>A (p.Arg208His)not specified [RCV004289584]uncertain significance13113650497113650497Humanname
401734590CV2709548single nucleotide variantNM_000705.4(ATP4B):c.424T>G (p.Phe142Val)not specified [RCV004318782]uncertain significance13113653004113653004Humanname
401721430CV2709958single nucleotide variantNM_000705.4(ATP4B):c.769G>A (p.Ala257Thr)not specified [RCV004315027]likely benign13113649481113649481Humanname
401865030CV2791455single nucleotide variantNM_000705.4(ATP4B):c.497C>A (p.Ala166Glu)not specified [RCV004358844]uncertain significance13113652931113652931Humanname
405665915CV3286940single nucleotide variantNM_000705.4(ATP4B):c.497C>T (p.Ala166Val)not specified [RCV004418504]likely benign13113652931113652931Humanname
405665927CV3286942single nucleotide variantNM_000705.4(ATP4B):c.807C>A (p.His269Gln)not specified [RCV004418506]uncertain significance13113649443113649443Humanname
405665932CV3286943single nucleotide variantNM_000705.4(ATP4B):c.857A>G (p.Lys286Arg)not specified [RCV004418507]uncertain significance13113649393113649393Humanname
407461745CV3488802single nucleotide variantNM_000705.4(ATP4B):c.362C>T (p.Ser121Phe)not specified [RCV004687731]uncertain significance13113653066113653066Humanname
407527655CV3488812single nucleotide variantNM_000705.4(ATP4B):c.667G>A (p.Gly223Ser)not specified [RCV004680088]uncertain significance13113650453113650453Humanname
407527666CV3488817single nucleotide variantNM_000705.4(ATP4B):c.712C>G (p.Gln238Glu)not specified [RCV004680093]uncertain significance13113650408113650408Humanname
597785253CV3616610single nucleotide variantNM_000705.4(ATP4B):c.584C>T (p.Ser195Leu)not specified [RCV004875034]uncertain significance13113651699113651699Humanname
597785262CV3616623single nucleotide variantNM_000705.4(ATP4B):c.343G>A (p.Ala115Thr)not specified [RCV004875036]likely benign13113653333113653333Humanname
597785265CV3616629single nucleotide variantNM_000705.4(ATP4B):c.549G>C (p.Met183Ile)not specified [RCV004875037]uncertain significance13113652879113652879Humanname
597785269CV3616639single nucleotide variantNM_000705.4(ATP4B):c.580G>A (p.Gly194Ser)not specified [RCV004875038]likely benign13113651703113651703Humanname
598183833CV3913295single nucleotide variantNM_000705.4(ATP4B):c.764G>A (p.Arg255Lys)not specified [RCV005287183]likely benign13113649486113649486Humanname
598183854CV3913302single nucleotide variantNM_000705.4(ATP4B):c.427C>T (p.Arg143Cys)not specified [RCV005287187]uncertain significance13113653001113653001Humanname
598165866CV3913308single nucleotide variantNM_000705.4(ATP4B):c.428G>A (p.Arg143His)not specified [RCV005283527]uncertain significance13113653000113653000Humanname
598183917CV3913317single nucleotide variantNM_000705.4(ATP4B):c.395C>T (p.Thr132Ile)not specified [RCV005287197]uncertain significance13113653033113653033Humanname
598165909CV3913326single nucleotide variantNM_000705.4(ATP4B):c.760C>T (p.Pro254Ser)not specified [RCV005283533]uncertain significance13113649490113649490Humanname