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WormBase Tree Display for Variation: WBVar01725449

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Name Class

WBVar01725449NamePublic_nameWBVar01725449
Other_namecewivar00423780
C34H4.1a.2:c.96C>T
C34H4.1a.1:c.96C>T
CE25804:p.Val32=
HGVSgCHROMOSOME_IV:g.1555675C>T
Sequence_detailsSMapS_parentSequenceC34H4
Flanking_sequencesAGTTTTCGAGTTGTACAAATTTGCTGGCGTGGGCCAACTAAAATAGGAAATGTAGATGTA
Mapping_targetC34H4
Source_location225CHROMOSOME_IV15556741555674From_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
AffectsGeneWBGene00016424
TranscriptC34H4.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC34H4.1a.1:c.96C>T
HGVSpCE25804:p.Val32=
cDNA_position97
CDS_position96
Protein_position32
Exon_number2/9
Codon_changegtC/gtT
Amino_acid_changeV
C34H4.1a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC34H4.1a.2:c.96C>T
HGVSpCE25804:p.Val32=
cDNA_position96
CDS_position96
Protein_position32
Exon_number1/8
Codon_changegtC/gtT
Amino_acid_changeV
MethodWGS_Flibotte