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Variants search result for Homo sapiens
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39 records found for search term Gna15
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155919142CV2202396single nucleotide variantNM_002068.4(GNA15):c.23G>A (p.Arg8His)not specified [RCV004080710]uncertain significance1931364733136473Humanname
156078432CV2289469single nucleotide variantNM_002068.4(GNA15):c.11C>T (p.Ser4Leu)not specified [RCV004152412]uncertain significance1931364613136461Humanname
155986026CV2344015single nucleotide variantNM_002068.4(GNA15):c.48G>C (p.Glu16Asp)not specified [RCV004195630]uncertain significance1931364983136498Humanname
597788584CV3678190single nucleotide variantNM_002068.4(GNA15):c.97T>G (p.Leu33Val)not specified [RCV004932733]uncertain significance1931365473136547Humanname
597730293CV3678192single nucleotide variantNM_002068.4(GNA15):c.68G>A (p.Arg23Gln)not specified [RCV004919808]uncertain significance1931365183136518Humanname
15162802CV716349single nucleotide variantNM_002068.4(GNA15):c.813C>T (p.Ser271=)not provided [RCV000970345]benign1931577963157796Humanname
155982252CV2351545single nucleotide variantNM_002068.4(GNA15):c.202G>A (p.Ala68Thr)not specified [RCV004193222]uncertain significance1931486473148647Humanname
329392859CV2469004single nucleotide variantNM_002068.4(GNA15):c.278T>C (p.Met93Thr)not specified [RCV004274262]uncertain significance1931487233148723Humanname
405768043CV3262042single nucleotide variantNM_002068.4(GNA15):c.205G>A (p.Gly69Ser)not specified [RCV004395431]uncertain significance1931486503148650Humanname
405768049CV3262043single nucleotide variantNM_002068.4(GNA15):c.212C>T (p.Ser71Leu)not specified [RCV004395432]uncertain significance1931486573148657Humanname
405768056CV3262044single nucleotide variantNM_002068.4(GNA15):c.215A>T (p.Glu72Val)not specified [RCV004395433]uncertain significance1931486603148660Humanname
597788580CV3678191single nucleotide variantNM_002068.4(GNA15):c.262G>C (p.Val88Leu)not specified [RCV004932734]uncertain significance1931487073148707Humanname
597730314CV3678194single nucleotide variantNM_002068.4(GNA15):c.119G>A (p.Arg40His)not specified [RCV004919810]uncertain significance1931365693136569Humanname
598264092CV3974344single nucleotide variantNM_002068.4(GNA15):c.289A>G (p.Met97Val)not specified [RCV005348762]uncertain significance1931487343148734Humanname
155976795CV2246081single nucleotide variantNM_002068.4(GNA15):c.505C>T (p.Arg169Cys)not specified [RCV004113988]uncertain significance1931517263151726Humanname
156132539CV2350145single nucleotide variantNM_002068.4(GNA15):c.544G>A (p.Val182Met)not specified [RCV004200065]uncertain significance1931517653151765Humanname
156056513CV2371090single nucleotide variantNM_002068.4(GNA15):c.595G>A (p.Val199Met)not specified [RCV004220843]uncertain significance1931518163151816Humanname
329382429CV2465228single nucleotide variantNM_002068.4(GNA15):c.467T>A (p.Leu156Gln)not specified [RCV004287261]uncertain significance1931502673150267Humanname
401734205CV2688430single nucleotide variantNM_002068.4(GNA15):c.604A>G (p.Thr202Ala)not specified [RCV004301415]uncertain significance1931518253151825Humanname
401777135CV2707747single nucleotide variantNM_002068.4(GNA15):c.496C>T (p.His166Tyr)not specified [RCV004306998]uncertain significance1931517173151717Humanname
401738200CV2711674single nucleotide variantNM_002068.4(GNA15):c.749G>A (p.Arg250His)not specified [RCV004309350]uncertain significance1931577323157732Humanname
401892785CV2762010single nucleotide variantNM_002068.4(GNA15):c.848A>G (p.Glu283Gly)not specified [RCV004339626]uncertain significance1931578313157831Humanname
401880042CV2765157single nucleotide variantNM_002068.4(GNA15):c.976G>T (p.Gly326Cys)not specified [RCV004339689]uncertain significance1931628703162870Humanname
401890371CV2768147single nucleotide variantNM_002068.4(GNA15):c.550C>T (p.Arg184Cys)not specified [RCV004350161]uncertain significance1931517713151771Humanname
405768062CV3262045single nucleotide variantNM_002068.4(GNA15):c.504G>T (p.Glu168Asp)not specified [RCV004395434]uncertain significance1931517253151725Humanname
597730284CV3678187single nucleotide variantNM_002068.4(GNA15):c.961A>C (p.Thr321Pro)not specified [RCV004919807]uncertain significance1931628553162855Humanname
597788588CV3678189single nucleotide variantNM_002068.4(GNA15):c.752T>G (p.Met251Arg)not specified [RCV004932732]uncertain significance1931577353157735Humanname
597730304CV3678193single nucleotide variantNM_002068.4(GNA15):c.929G>A (p.Arg310Lys)not specified [RCV004919809]uncertain significance1931628233162823Humanname
598264082CV3974341single nucleotide variantNM_002068.4(GNA15):c.307C>G (p.Pro103Ala)not specified [RCV005348759]uncertain significance1931487523148752Humanname
598264089CV3974343single nucleotide variantNM_002068.4(GNA15):c.971T>G (p.Val324Gly)not specified [RCV005348761]uncertain significance1931628653162865Humanname
598264094CV3974345single nucleotide variantNM_002068.4(GNA15):c.904A>G (p.Lys302Glu)not specified [RCV005348763]uncertain significance1931627983162798Humanname
598264097CV3974346single nucleotide variantNM_002068.4(GNA15):c.613C>T (p.Arg205Trp)not specified [RCV005348764]uncertain significance1931518343151834Humanname
598264100CV3974347single nucleotide variantNM_002068.4(GNA15):c.680T>A (p.Ile227Asn)not specified [RCV005348765]uncertain significance1931558883155888Humanname
15156433CV716347single nucleotide variantNM_002068.4(GNA15):c.341G>A (p.Ser114Asn)not provided [RCV000969111]benign1931501413150141Humanname
15176594CV716348single nucleotide variantNM_002068.4(GNA15):c.561G>A (p.Met187Ile)not provided [RCV000973222]benign1931517823151782Humanname
8628264CV83408single nucleotide variantNM_002068.3(GNA15):c.517G>A (p.Glu173Lys)Malignant melanoma [RCV000063488]not provided1931517383151738Humanname
597788593CV3678188single nucleotide variantNM_002068.4(GNA15):c.1012C>T (p.Arg338Cys)not specified [RCV004932731]uncertain significance1931629063162906Humanname
598264085CV3974342single nucleotide variantNM_002068.4(GNA15):c.1057C>T (p.Arg353Cys)not specified [RCV005348760]uncertain significance1931629513162951Humanname
8628265CV83409single nucleotide variantNM_002068.3(GNA15):c.1096C>T (p.Arg366Cys)Malignant melanoma [RCV000063489]not provided1931629903162990Humanname