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WormBase Tree Display for Variation: WBVar01547075

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Name Class

WBVar01547075NamePublic_nameWBVar01547075
Other_namecewivar00121842
C05D12.3c.3:c.1048C>T
C05D12.3c.2:c.1048C>T
C05D12.3a.1:c.1048C>T
CE39469:p.Leu350=
CE36974:p.Leu350=
C05D12.3c.1:c.1048C>T
HGVSgCHROMOSOME_II:g.11427374C>T
Sequence_detailsSMapS_parentSequenceC05D12
Flanking_sequencesGACTAGCAGAAAAGTACTCTCCACTTACAGTAGTCGCCGGACAGAACATGAAAGTTGTCA
Mapping_targetC05D12
Source_location225CHROMOSOME_II1142731011427310From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00014666
TranscriptC05D12.3a.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC05D12.3a.1:c.1048C>T
HGVSpCE36974:p.Leu350=
cDNA_position1060
CDS_position1048
Protein_position350
Exon_number6/16
Codon_changeCta/Tta
Amino_acid_changeL
C05D12.3c.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC05D12.3c.1:c.1048C>T
HGVSpCE39469:p.Leu350=
cDNA_position1063
CDS_position1048
Protein_position350
Exon_number6/18
Codon_changeCta/Tta
Amino_acid_changeL
C05D12.3c.3VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC05D12.3c.3:c.1048C>T
HGVSpCE39469:p.Leu350=
cDNA_position1048
CDS_position1048
Protein_position350
Exon_number5/18
Codon_changeCta/Tta
Amino_acid_changeL
C05D12.3c.2VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC05D12.3c.2:c.1048C>T
HGVSpCE39469:p.Leu350=
cDNA_position1062
CDS_position1048
Protein_position350
Exon_number6/17
Codon_changeCta/Tta
Amino_acid_changeL
MethodWGS_Flibotte