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WormBase Tree Display for Variation: WBVar01454367

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Name Class

WBVar01454367EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01454367
Other_namecewivar00572218
C29E6.1b.1:c.801G>A
CE37323:p.Gln267=
C29E6.1a.1:c.801G>A
CE05332:p.Gln267=
CE40548:p.Gln267=
C29E6.1c.1:c.801G>A
HGVSgCHROMOSOME_IV:g.11886936G>A
Sequence_detailsSMapS_parentSequenceC29E6
Flanking_sequencesCACTGAATTCGATCACTTTTTCCCATATCAACTGTCAGCAAGAACTGTTCGGATTCTATT
Mapping_targetC29E6
Type_of_mutationSubstitutionga
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00023084From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193340024
dbSNP_ssss295515943
StatusLive
AffectsGeneWBGene00002827
TranscriptC29E6.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29E6.1b.1:c.801G>A
HGVSpCE37323:p.Gln267=
cDNA_position806
CDS_position801
Protein_position267
Exon_number5/11
Codon_changecaG/caA
Amino_acid_changeQ
C29E6.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29E6.1a.1:c.801G>A
HGVSpCE40548:p.Gln267=
cDNA_position804
CDS_position801
Protein_position267
Exon_number5/12
Codon_changecaG/caA
Amino_acid_changeQ
C29E6.1c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29E6.1c.1:c.801G>A
HGVSpCE05332:p.Gln267=
cDNA_position801
CDS_position801
Protein_position267
Exon_number4/10
Codon_changecaG/caA
Amino_acid_changeQ
ReferenceWBPaper00040707
MethodWGS_Andersen