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WormBase Tree Display for Variation: WBVar01826684

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Name Class

WBVar01826684NamePublic_nameWBVar01826684
Other_namecewivar00538674
F29C12.3c.1:c.50+1809C>G
F29C12.1b.1:c.306G>C
F29C12.3b.1:c.2486+1809C>G
CE37902:p.Gln102His
CE19820:p.Gln102His
F29C12.3a.1:c.2480+1809C>G
F29C12.1a.1:c.306G>C
HGVSgCHROMOSOME_II:g.13108378G>C
Sequence_detailsSMapS_parentSequenceF29C12
Flanking_sequencesCGAGGGAGGGCCACAGGTTCAGAGACCACAGTGGGATTTTGAATTGAAAAAAAAATTTAT
Mapping_targetF29C12
Source_location225CHROMOSOME_II1310830813108308From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022886From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004120
WBGene00009245
TranscriptF29C12.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF29C12.3b.1:c.2486+1809C>G
Intron_number11/17
F29C12.1a.1 (12)
F29C12.1b.1 (12)
F29C12.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF29C12.3c.1:c.50+1809C>G
Intron_number1/6
F29C12.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF29C12.3a.1:c.2480+1809C>G
Intron_number11/17
MethodWGS_Flibotte