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WormBase Tree Display for Variation: WBVar00036411

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Name Class

WBVar00036411NamePublic_nameWBVar00036411
Other_name (13)
HGVSgCHROMOSOME_II:g.1227538G>A
Sequence_detailsSMapS_parentSequenceF47F6
Flanking_sequencestaccgcactagccgaccgcccatcggcttcccggatggctaagctgctctgcgaggagatcaccactgagcagttctctccggtggcattccccggtggttctgagcttattgtacagtatgatgagcatgtgctcacgaatacctataaatttggagttatctatcaaaaaggcggacagacgactgaggagcaacttttcggaaatccacacgggagcccggcttttgacgagtttttgtcgatgattggcgattctgtgcagttgaatggctttcaggtaggcaaattgagcggcaatttgatctctagaaatttaatctccgcccacaaaatggcattggtttctaaaactccaaaaattcaaaaaaaaaatcgacaaagaagtttcgaaaaaaaattcttcctcaaaattaaaattttttgaagaatatgttttgtggttacagactccgcccacaaatgggcggggcttcaccgactccgcccacacaatgacaattatttatcccaaaaaattgggtcacaaaaccacagtttctcatcaagttgtctaacttttccattcgtgaaaagtaagaaaaggggcggagcttagga
Mapping_targetF47F6
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (17)
LaboratoryAX
PersonWBPerson6900
WBPerson4037
AnalysisWGS_Pasadena_Quinlan
WGS_De_Bono
WGS_Yanai
Million_mutation_project_reanalysis
SNP_Swan
HistoryAcquires_mergeWBVar01294316
WBVar00544734
WBVar01359963
WBVar00267904
StatusLive
AffectsGeneWBGene00018734
TranscriptF53A10.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A10.2d.1:c.834+21G>A
Intron_number5/9
F53A10.2b.4VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A10.2b.4:c.-82+21G>A
Intron_number2/8
F53A10.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A10.2c.1:c.1224+21G>A
Intron_number4/8
F53A10.2b.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A10.2b.3:c.-82+21G>A
Intron_number5/11
F53A10.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A10.2b.1:c.-82+21G>A
Intron_number6/12
F53A10.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A10.2e.1:c.615+21G>A
Intron_number3/7
F53A10.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A10.2f.1:c.549+21G>A
Intron_number2/6
F53A10.2b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A10.2b.2:c.-82+21G>A
Intron_number4/10
F53A10.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A10.2a.1:c.1017+21G>A
Intron_number7/12
ReferenceWBPaper00038208
WBPaper00037807
WBPaper00005369
MethodWGS_Pasadena_Quinlan