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WormBase Tree Display for Variation: WBVar01744375

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Name Class

WBVar01744375NamePublic_nameWBVar01744375
Other_namecewivar00443659
T16A9.3.3:c.441C>T
T16A9.3.2:c.441C>T
T16A9.3.1:c.441C>T
CE43662:p.His147=
HGVSgCHROMOSOME_V:g.14208151C>T
Sequence_detailsSMapS_parentSequenceT16A9
Flanking_sequencesTTATTACCAATTTAATTCCAGATCCCGCCAAATTTGATGCTAAAAACATCCGACGGCGTC
Mapping_targetT16A9
Source_location225CHROMOSOME_V1420813614208136From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00011793
TranscriptT16A9.3.3VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT16A9.3.3:c.441C>T
HGVSpCE43662:p.His147=
cDNA_position1172
CDS_position441
Protein_position147
Exon_number5/9
Codon_changecaC/caT
Amino_acid_changeH
T16A9.3.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT16A9.3.2:c.441C>T
HGVSpCE43662:p.His147=
cDNA_position591
CDS_position441
Protein_position147
Exon_number4/8
Codon_changecaC/caT
Amino_acid_changeH
T16A9.3.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT16A9.3.1:c.441C>T
HGVSpCE43662:p.His147=
cDNA_position899
CDS_position441
Protein_position147
Exon_number6/10
Codon_changecaC/caT
Amino_acid_changeH
MethodWGS_Flibotte