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WormBase Tree Display for Variation: WBVar01609662

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Name Class

WBVar01609662NamePublic_nameWBVar01609662
Other_namecewivar00288852
M02H5.3.2:c.1224C>T
M02H5.3.1:c.1224C>T
CE50748:p.His408=
HGVSgCHROMOSOME_V:g.467345C>T
Sequence_detailsSMapS_parentSequenceM02H5
Flanking_sequencesGTTCAAAGTGTGTTTCGCTAAATACTCGCACCGGAATTATTTTTTGAATACGAATAAGTG
Mapping_targetM02H5
Source_location225CHROMOSOME_V467346467346From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019741
TranscriptM02H5.3.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScM02H5.3.2:c.1224C>T
HGVSpCE50748:p.His408=
cDNA_position1797
CDS_position1224
Protein_position408
Exon_number8/9
Codon_changecaC/caT
Amino_acid_changeH
M02H5.3.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScM02H5.3.1:c.1224C>T
HGVSpCE50748:p.His408=
cDNA_position1275
CDS_position1224
Protein_position408
Exon_number9/10
Codon_changecaC/caT
Amino_acid_changeH
MethodWGS_Flibotte