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WormBase Tree Display for Variation: WBVar00584124

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Name Class

WBVar00584124EvidencePaper_evidenceWBPaper00038208
NamePublic_nameWBVar00584124
Other_namehaw164259
cewivar00229534
T27C4.4d.1:c.*367C>G
T27C4.4a.1:c.2608-207C>G
T27C4.4b.1:c.2607+373C>G
T27C4.4e.1:c.2202+373C>G
T27C4.4b.2:c.2607+373C>G
HGVSgCHROMOSOME_V:g.3710491C>G
Sequence_detailsSMapS_parentSequenceT27C4
Flanking_sequencesTTGTAGATCAACGTAGATCAAGCCTAAATCAGACACCCTGAAACACACACACGAGTGAAAAATGAACAATGTGTGCGATTTTCCGAATCCTAACCGCCCG
Mapping_targetT27C4
Type_of_mutationSubstitutioncg
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WGS_Yanai
PersonWBPerson4037
AnalysisWGS_Yanai
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003025
TranscriptT27C4.4d.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScT27C4.4d.1:c.*367C>G
cDNA_position3004
Exon_number8/9
T27C4.4b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4b.2:c.2607+373C>G
Intron_number7/8
T27C4.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4a.1:c.2608-207C>G
Intron_number7/9
T27C4.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4e.1:c.2202+373C>G
Intron_number4/4
T27C4.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4b.1:c.2607+373C>G
Intron_number7/8
ReferenceWBPaper00038208
MethodWGS_Yanai