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WormBase Tree Display for Variation: WBVar00227856

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Name Class

WBVar00227856EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar00227856
Other_namepas39632
cewivar00093378
M176.6b.1:c.1101-13T>A
M176.6a.1:c.1281-13T>A
HGVSgCHROMOSOME_II:g.9431694A>T
Sequence_detailsSMapS_parentSequenceM176
Flanking_sequencescatctttattcaaaagccaaactaaaatagaaaaataaaaaaagccattagtctctccgaatccaatcctctaatttgctctgtcgttccgcttctgatttcagcgttttttgaatttgttccagaagctgaaatttaaaaaaatcatatttaaaataacttgaaatattttttaatcttacgttagtagcagatacactcaaatgttcttcgaagaattccacacacttggagaagctgggtcgaaatgttgcatcgaaattccaaaattgtttcattcgatcgtacctaaatttttttaaagttttattctagaagtttgagtttcccagcgattgattatgctaacattttaggatgacaatactgtggcattggaagttgatttccctgaacaacatgctcaaaaacatcactgttggatacatttgaatatggtaattctcccaatgagaacatttcataaagactaacaccatacgaccacacatccgatttttctgtgcattttccttctctcataacttctggagccatccatctagcaggcataggagttcctacacctttcgttattctgaaaattttatgtaatgttta
Mapping_targetM176
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (36)
LaboratoryQX
PersonWBPerson6900
WBPerson1730
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
WGS_Andersen
HistoryAcquires_mergeWBVar01439088
StatusLive
AffectsGeneWBGene00002199
TranscriptM176.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM176.6b.1:c.1101-13T>A
Intron_number7/9
M176.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM176.6a.1:c.1281-13T>A
Intron_number8/10
ReferenceWBPaper00040707
MethodWGS_Pasadena_Quinlan