Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01749377

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01749377NamePublic_nameWBVar01749377
Other_namecewivar00448844
Y59A8B.14b.1:c.678-224C>T
Y59A8B.14c.1:c.1089-224C>T
Y59A8B.14a.1:c.1101-224C>T
HGVSgCHROMOSOME_V:g.18103982C>T
Sequence_detailsSMapS_parentSequenceY59A8B
Flanking_sequencesAAAATTTGGAAAAAATCGGTTTTTTTCTTTATTTTCAATCTAAAACTTAATGATACAAAA
Mapping_targetY59A8B
Source_location225CHROMOSOME_V1810395418103954From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003919
TranscriptY59A8B.14a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.14a.1:c.1101-224C>T
Intron_number7/10
Y59A8B.14b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.14b.1:c.678-224C>T
Intron_number4/7
Y59A8B.14c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.14c.1:c.1089-224C>T
Intron_number7/10
MethodWGS_Flibotte