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WormBase Tree Display for Variation: WBVar01468943

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Name Class

WBVar01468943EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01468943
Other_namecewivar00126729
CE54583:p.Ser412=
CE28488:p.Ser398=
T23F2.1b.1:c.1236A>T
T23F2.1a.1:c.1194A>T
HGVSgCHROMOSOME_X:g.5495427A>T
Sequence_detailsSMapS_parentSequenceT23F2
Flanking_sequencesCGAAATGATGGGAACGTTGGAGATCAGCTCTCGGAGCCAACGACAACGCCGCTCGTGGAC
Mapping_targetT23F2
Type_of_mutationSubstitutionat
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004445From_analysisWGS_Andersen
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00004603From_analysisWGS_Andersen
WBStrain00005305From_analysisWGS_Andersen
WBStrain00005315From_analysisWGS_Andersen
WBStrain00006369From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193354245
dbSNP_ssss295530164
StatusLive
AffectsGeneWBGene00044623
TranscriptT23F2.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT23F2.1b.1:c.1236A>T
HGVSpCE54583:p.Ser412=
cDNA_position1236
CDS_position1236
Protein_position412
Exon_number9/9
Codon_changetcA/tcT
Amino_acid_changeS
T23F2.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT23F2.1a.1:c.1194A>T
HGVSpCE28488:p.Ser398=
cDNA_position1194
CDS_position1194
Protein_position398
Exon_number8/9
Codon_changetcA/tcT
Amino_acid_changeS
ReferenceWBPaper00040707
MethodWGS_Andersen