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WormBase Tree Display for Variation: WBVar01623701

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Name Class

WBVar01623701NamePublic_nameWBVar01623701
Other_namecewivar00303663
CE13361:p.Ala308=
T07D3.4a.1:c.924C>T
T07D3.4b.1:c.369C>T
CE51164:p.Ala123=
HGVSgCHROMOSOME_II:g.890188C>T
Sequence_detailsSMapS_parentSequenceT07D3
Flanking_sequencesACTTACCCATCATTGGGTGGGCGGAATTGCAGTGAGTTACTGTAGGGGGTACTGTACAAG
Mapping_targetT07D3
Source_location225CHROMOSOME_II890195890195From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00020307
TranscriptT07D3.4b.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScT07D3.4b.1:c.369C>T
HGVSpCE51164:p.Ala123=
cDNA_position369
CDS_position369
Protein_position123
Exon_number2/4
Codon_changegcC/gcT
Amino_acid_changeA
T07D3.4a.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScT07D3.4a.1:c.924C>T
HGVSpCE13361:p.Ala308=
cDNA_position1067
CDS_position924
Protein_position308
Exon_number8/11
Codon_changegcC/gcT
Amino_acid_changeA
MethodWGS_Flibotte