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WormBase Tree Display for Variation: WBVar01533980

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Name Class

WBVar01533980NamePublic_nameWBVar01533980
Other_namecewivar00080101
F56D12.1c.1:c.411A>C
F56D12.1b.1:c.411A>C
CE33403:p.Gly137=
F56D12.1a.1:c.411A>C
CE29047:p.Gly137=
F56D12.1a.2:c.411A>C
CE37118:p.Gly137=
HGVSgCHROMOSOME_II:g.1309012T>G
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesCGTGGAGGCGTTCAGCTTCATTCGGTACTTCCAGCGGCCAAATCGGCGGCGCGGAGCAAA
Mapping_targetF56D12
Source_location225CHROMOSOME_II13090191309019From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000112
TranscriptF56D12.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1b.1:c.411A>C
HGVSpCE33403:p.Gly137=
cDNA_position413
CDS_position411
Protein_position137
Exon_number5/8
Codon_changeggA/ggC
Amino_acid_changeG
F56D12.1a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.2:c.411A>C
HGVSpCE29047:p.Gly137=
cDNA_position510
CDS_position411
Protein_position137
Exon_number6/10
Codon_changeggA/ggC
Amino_acid_changeG
F56D12.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.1:c.411A>C
HGVSpCE29047:p.Gly137=
cDNA_position414
CDS_position411
Protein_position137
Exon_number5/9
Codon_changeggA/ggC
Amino_acid_changeG
F56D12.1c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1c.1:c.411A>C
HGVSpCE37118:p.Gly137=
cDNA_position411
CDS_position411
Protein_position137
Exon_number4/6
Codon_changeggA/ggC
Amino_acid_changeG
MethodWGS_Flibotte