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WormBase Tree Display for Variation: WBVar01698008

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Name Class

WBVar01698008NamePublic_nameWBVar01698008
Other_namecewivar00394798
C29F9.6.2:c.408T>C
CE43673:p.Val136=
C29F9.6.1:c.408T>C
C29F9.6.3:c.408T>C
HGVSgCHROMOSOME_III:g.116132T>C
Sequence_detailsSMapS_parentSequenceC29F9
Flanking_sequencesAGGAACCTCACAACCGTGGCACAGTGAAGTCCGAAAACCGATAGAGAGGCAGTTATTGAG
Mapping_targetC29F9
Source_location225CHROMOSOME_III116131116131From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00016221
TranscriptC29F9.6.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29F9.6.1:c.408T>C
HGVSpCE43673:p.Val136=
cDNA_position580
CDS_position408
Protein_position136
Exon_number7/9
Codon_changegtT/gtC
Amino_acid_changeV
C29F9.6.3VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29F9.6.3:c.408T>C
HGVSpCE43673:p.Val136=
cDNA_position503
CDS_position408
Protein_position136
Exon_number6/8
Codon_changegtT/gtC
Amino_acid_changeV
C29F9.6.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29F9.6.2:c.408T>C
HGVSpCE43673:p.Val136=
cDNA_position555
CDS_position408
Protein_position136
Exon_number5/7
Codon_changegtT/gtC
Amino_acid_changeV
MethodWGS_Flibotte