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WormBase Tree Display for Variation: WBVar00002451

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Name Class

WBVar00002451NamePublic_nameWBVar00002451
Other_namepas12087
cewivar00066024
F56C11.1.1:c.298+15C>T
F56C11.1.2:c.298+15C>T
HGVSgCHROMOSOME_I:g.153380G>A
Sequence_detailsSMapS_parentSequenceF56C11
Flanking_sequencesagatcttaatgaggacacccatggctgggtggtaccatagatgaatgatccatcaatccatgaagtccgttcattgatttgttctcgaggtgagttgagcccatttccagttgctttatcgtatttggcacgtgtaaatgggatttctgtctttccctcacattctttatcaaatacattatcacataggggtacttgaattttaagtgtctctagtggacaggatactccatttgattgcattatttcataagcaactacttgacctataattattattactaatttttgaggtagaggcaataaaaacgaactgaaaaatgccaataaagtcgtgcatcctcttgtattaggtataccggactctcctttgaatagtatatcggagagttcacgggcggacggaagtgagttattcactgaatatacaccgtctgagtagtaggaacgtgcatctctatgcagccgacttcctgaaggagtaggtcaatgtaacgtcatttctcttccgaaaaaacctaccagcagaaccccattcactattcgccagattgttgtaccatccgtcgtatctttgaaattcctcattttgttggattc
Mapping_targetF56C11
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (15)
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000253
TranscriptF56C11.1.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56C11.1.1:c.298+15C>T
Intron_number4/20
F56C11.1.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56C11.1.2:c.298+15C>T
Intron_number4/20
MethodWGS_Pasadena_Quinlan