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: WBVar01822308

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01822308NamePublic_nameWBVar01822308
Other_namecewivar00534069
Y41G9A.4a.1:c.1342-264A>T
Y41G9A.4c.1:c.1342-264A>T
Y41G9A.4d.1:c.1342-264A>T
Y41G9A.4b.1:c.1342-264A>T
HGVSgCHROMOSOME_X:g.2961074A>T
Sequence_detailsSMapS_parentSequenceY41G9A
Flanking_sequencesGAGATTTCAGCTAAAATTGAGCCTTTTTTTAATTTTGAACCGCTATGAAAAACTTTTGAA
Mapping_targetY41G9A
Source_location225CHROMOSOME_X29610642961064From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022868From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021528
TranscriptY41G9A.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4c.1:c.1342-264A>T
Intron_number10/20
Y41G9A.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4a.1:c.1342-264A>T
Intron_number9/11
Y41G9A.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4d.1:c.1342-264A>T
Intron_number9/19
Y41G9A.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4b.1:c.1342-264A>T
Intron_number10/21
MethodWGS_Flibotte