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WormBase Tree Display for Variation: WBVar01450798

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Name Class

WBVar01450798EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01450798
Other_namecewivar00566186
Y41D4B.33:n.12T>A
CE48212:p.Phe223Tyr
Y41D4B.19b.1:c.3560T>A
Y41D4B.19c.1:c.668T>A
CE52059:p.Phe1187Tyr
HGVSgCHROMOSOME_IV:g.1569792A>T
Sequence_detailsSMapS_parentSequenceY41D4B
Flanking_sequencesGGAAAGTATTTAGTGTCTCTGTAGACTGAGAGAGCTCTCCAATTGTATTTGAAAGTTGCT
Mapping_targetY41D4B
Type_of_mutationSubstitutionat
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00005835From_analysisWGS_Andersen
WBStrain00022898From_analysisWGS_Andersen
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00023084From_analysisWGS_Andersen
WBStrain00023152From_analysisWGS_Andersen
WBStrain00023164From_analysisWGS_Andersen
WBStrain00023176From_analysisWGS_Andersen
WBStrain00023177From_analysisWGS_Andersen
WBStrain00031279From_analysisWGS_Andersen
WBStrain00031284From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193336455
dbSNP_ssss295512374
StatusLive
AffectsGeneWBGene00003794
WBGene00220152
TranscriptY41D4B.19c.1 (12)
Y41D4B.19b.1 (12)
Y41D4B.33VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScY41D4B.33:n.12T>A
cDNA_position12
Exon_number1/1
ReferenceWBPaper00040707
MethodWGS_Andersen