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WormBase Tree Display for Variation: WBVar01698170

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Name Class

WBVar01698170NamePublic_nameWBVar01698170
Other_namecewivar00394965
C29F9.3c.1:c.414G>A
CE28896:p.Ala155=
C29F9.3a.1:c.465G>A
CE30624:p.Ala138=
C29F9.3b.1:c.*331G>A
C29F9.3a.2:c.465G>A
HGVSgCHROMOSOME_III:g.125876G>A
Sequence_detailsSMapS_parentSequenceC29F9
Flanking_sequencesATTTCAAACCATTTTATACTGGACCAATGCATTAGGACAAATATGTCGATCATTGGAGCT
Mapping_targetC29F9
Source_location225CHROMOSOME_III125875125875From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
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
AffectsGeneWBGene00016218
TranscriptC29F9.3b.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScC29F9.3b.1:c.*331G>A
cDNA_position607
Exon_number5/6
C29F9.3a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29F9.3a.1:c.465G>A
HGVSpCE28896:p.Ala155=
cDNA_position492
CDS_position465
Protein_position155
Exon_number4/9
Codon_changegcG/gcA
Amino_acid_changeA
C29F9.3c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29F9.3c.1:c.414G>A
HGVSpCE30624:p.Ala138=
cDNA_position428
CDS_position414
Protein_position138
Exon_number5/8
Codon_changegcG/gcA
Amino_acid_changeA
C29F9.3a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29F9.3a.2:c.465G>A
HGVSpCE28896:p.Ala155=
cDNA_position479
CDS_position465
Protein_position155
Exon_number4/9
Codon_changegcG/gcA
Amino_acid_changeA
MethodWGS_Flibotte