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WormBase Tree Display for Variation: WBVar01671544

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Name Class

WBVar01671544NamePublic_nameWBVar01671544
Other_namecewivar00361550
CE19743:p.Leu810=
CE50538:p.Leu163=
C49C3.4b.1:c.676T>C
C49C3.4a.1:c.2428T>C
C49C3.4c.1:c.487T>C
CE48513:p.Leu226=
HGVSgCHROMOSOME_IV:g.17324699T>C
Sequence_detailsSMapS_parentSequenceC49C3
Flanking_sequencesTTTGTCAGAAACATTGGTTCAAATAGATTCTATCACTTGGAAGTTCCATTGGAACTTTAA
Mapping_targetC49C3
Source_location225CHROMOSOME_IV1732466217324662From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022899From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00008194
TranscriptC49C3.4c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC49C3.4c.1:c.487T>C
HGVSpCE50538:p.Leu163=
cDNA_position487
CDS_position487
Protein_position163
Exon_number4/15
Codon_changeTta/Cta
Amino_acid_changeL
C49C3.4b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC49C3.4b.1:c.676T>C
HGVSpCE48513:p.Leu226=
cDNA_position676
CDS_position676
Protein_position226
Exon_number5/16
Codon_changeTta/Cta
Amino_acid_changeL
C49C3.4a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC49C3.4a.1:c.2428T>C
HGVSpCE19743:p.Leu810=
cDNA_position2431
CDS_position2428
Protein_position810
Exon_number12/24
Codon_changeTta/Cta
Amino_acid_changeL
MethodWGS_Flibotte