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WormBase Tree Display for Variation: WBVar01762694

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Name Class

WBVar01762694NamePublic_nameWBVar01762694
Other_namecewivar00462616
CE40074:p.Lys347=
F56D12.1b.1:c.1461G>A
F56D12.1a.1:c.1461G>A
F56D12.1d.1:c.1041G>A
CE29047:p.Lys487=
CE33403:p.Lys487=
F56D12.1a.2:c.1461G>A
HGVSgCHROMOSOME_II:g.1307184C>T
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesTTTTGTAGTTGCCAACCTATAAAGGAACTCTTATCCTGCGAAAAAACGGCGCCAGTCAGC
Mapping_targetF56D12
Source_location225CHROMOSOME_II13071911307191From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000112
TranscriptF56D12.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1b.1:c.1461G>A
HGVSpCE33403:p.Lys487=
cDNA_position1463
CDS_position1461
Protein_position487
Exon_number7/8
Codon_changeaaG/aaA
Amino_acid_changeK
F56D12.1a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.2:c.1461G>A
HGVSpCE29047:p.Lys487=
cDNA_position1560
CDS_position1461
Protein_position487
Exon_number8/10
Codon_changeaaG/aaA
Amino_acid_changeK
F56D12.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.1:c.1461G>A
HGVSpCE29047:p.Lys487=
cDNA_position1464
CDS_position1461
Protein_position487
Exon_number7/9
Codon_changeaaG/aaA
Amino_acid_changeK
F56D12.1d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1d.1:c.1041G>A
HGVSpCE40074:p.Lys347=
cDNA_position1041
CDS_position1041
Protein_position347
Exon_number3/4
Codon_changeaaG/aaA
Amino_acid_changeK
MethodWGS_Flibotte