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WormBase Tree Display for Variation: WBVar00065224

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Name Class

WBVar00065224EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar00065224
Other_namepas24642
cewivar00108053
F10E9.6c.1:c.449-1190A>G
F10E9.6a.3:c.113-1190A>G
F10E9.6a.1:c.113-1190A>G
F10E9.6a.2:c.113-1190A>G
HGVSgCHROMOSOME_III:g.8299160A>G
Sequence_detailsSMapS_parentSequenceF10E9
Flanking_sequencestcaaaactgacttttttttgtttctaagtaaagacttttgcggtaggtaggcaagccttacatttgcgcctaccacatgcccagtatgaagtcttgtgcttggtacaacatagatttttttaattggcatttttcttgaaaatttagtaaattttgaaaatattattacaattttgttgaaaacggcggataacgttttggcaatatcaaagctcaaaaaaaaatcaacaaaattttgaaaaataaatttttactgaaaacagaagcctgatctggaaatatgattaattagcttcttttatgacgtggacgttctatctacaatctgtcgcaattcgacctcatctatatcgcttctgtccgcctacttttgtgggctcttcctgctctccctctgtcactctatttctctcatcggtcagctgtgcacctgtctattatttgtgtgtcccctcctcttccatcatctcttaccactacttttctctgttattcttctcagcttaatgaggttttcaaatgatgcacagagattaactttgttttcattcaaaaccagtaattattgttattttttcaatacacaccactcaaaataat
Mapping_targetF10E9
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00004604From_analysisWGS_Pasadena_Quinlan
WBStrain00006642From_analysisWGS_De_Bono
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
WGS_De_Bono
Million_mutation_project_reanalysis
HistoryAcquires_mergeWBVar01266166
StatusLive
AffectsGeneWBGene00003243
TranscriptF10E9.6a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF10E9.6a.3:c.113-1190A>G
Intron_number4/12
F10E9.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF10E9.6a.1:c.113-1190A>G
Intron_number2/10
F10E9.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF10E9.6c.1:c.449-1190A>G
Intron_number3/10
F10E9.6a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF10E9.6a.2:c.113-1190A>G
Intron_number3/11
ReferenceWBPaper00037807
MethodWGS_Pasadena_Quinlan