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WormBase Tree Display for Variation: WBVar00271934

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Name Class

WBVar00271934EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00271934
Other_nameuCE5-1261
Y58A7A.3.1:c.1893T>C
Y58A7A.3.2:c.1893T>C
CE26196:p.Cys631=
HGVSgCHROMOSOME_V:g.5078736A>G
Sequence_detailsSMapS_parentSequenceY58A7A
Flanking_sequencesATCTCAGGTGCCACTTCTTTTCCCATTCAGCATAATTTTCACAATTCATTGGCCAATGAGGTACTCCCTTGCAATCCCGACACCAAGAATATCCACATGGCATGAACGATTTTGAGTTTTATTTTCATTCCCTGGTTCTTCGAAAAATATAGTTGACTTGCAAGAAGGGCACTTTTCAAAATCTCCAGTTGCACCAAGAT
Mapping_targetY58A7A
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
AnalysisSNP_Swan
StatusLive
AffectsGeneWBGene00021977
TranscriptY58A7A.3.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScY58A7A.3.1:c.1893T>C
HGVSpCE26196:p.Cys631=
cDNA_position1972
CDS_position1893
Protein_position631
Exon_number6/8
Codon_changetgT/tgC
Amino_acid_changeC
Y58A7A.3.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScY58A7A.3.2:c.1893T>C
HGVSpCE26196:p.Cys631=
cDNA_position1965
CDS_position1893
Protein_position631
Exon_number6/8
Codon_changetgT/tgC
Amino_acid_changeC
ReferenceWBPaper00005369
MethodSNP_Swan