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WormBase Tree Display for Variation: WBVar01623503

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Name Class

WBVar01623503NamePublic_nameWBVar01623503
Other_namecewivar00303457
T07D3.7a.1:c.1503G>C
CE32063:p.Ala501=
CE13367:p.Ala482=
T07D3.7b.1:c.1446G>C
HGVSgCHROMOSOME_II:g.876564G>C
Sequence_detailsSMapS_parentSequenceT07D3
Flanking_sequencesCCACACTGGAATGGAAGTCCGTACCTGGGCATTGCATGCTTTGCTCAGCAATCTCATGTC
Mapping_targetT07D3
Source_location225CHROMOSOME_II876571876571From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000106
TranscriptT07D3.7b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT07D3.7b.1:c.1446G>C
HGVSpCE13367:p.Ala482=
cDNA_position1448
CDS_position1446
Protein_position482
Exon_number5/8
Codon_changegcG/gcC
Amino_acid_changeA
T07D3.7a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT07D3.7a.1:c.1503G>C
HGVSpCE32063:p.Ala501=
cDNA_position1503
CDS_position1503
Protein_position501
Exon_number5/8
Codon_changegcG/gcC
Amino_acid_changeA
MethodWGS_Flibotte