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WormBase Tree Display for Variation: WBVar01262887

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Name Class

WBVar01262887EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01262887
Other_name (17)
HGVSgCHROMOSOME_III:g.4250991T>A
Sequence_detailsSMapS_parentSequenceT08A11
Flanking_sequencesTATTCAGCTTTGAATTTGAACATTTTCTTCGAGTTTAACGACGATTCCGACCGTATTTGCCTTCTGAACCTTATTTAACGATTATTACAGTACTTTTTTA
Mapping_targetT08A11
Type_of_mutationSubstitutiontAPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006642From_analysisWGS_De_Bono
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539098542
StatusLive
AffectsGeneWBGene00011604
TranscriptT08A11.1e.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT08A11.1e.1:c.4200A>T
HGVSpCE54607:p.Gly1400=
cDNA_position4200
CDS_position4200
Protein_position1400
Exon_number15/18
Codon_changeggA/ggT
Amino_acid_changeG
T08A11.1g.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT08A11.1g.1:c.4206A>T
HGVSpCE54616:p.Gly1402=
cDNA_position4302
CDS_position4206
Protein_position1402
Exon_number16/19
Codon_changeggA/ggT
Amino_acid_changeG
T08A11.1h.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT08A11.1h.1:c.4212A>T
HGVSpCE54610:p.Gly1404=
cDNA_position4308
CDS_position4212
Protein_position1404
Exon_number16/19
Codon_changeggA/ggT
Amino_acid_changeG
T08A11.1d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT08A11.1d.1:c.4206A>T
HGVSpCE54612:p.Gly1402=
cDNA_position4302
CDS_position4206
Protein_position1402
Exon_number16/19
Codon_changeggA/ggT
Amino_acid_changeG
T08A11.1f.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT08A11.1f.1:c.4206A>T
HGVSpCE54622:p.Gly1402=
cDNA_position4206
CDS_position4206
Protein_position1402
Exon_number15/18
Codon_changeggA/ggT
Amino_acid_changeG
T08A11.1c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT08A11.1c.1:c.4200A>T
HGVSpCE54609:p.Gly1400=
cDNA_position4200
CDS_position4200
Protein_position1400
Exon_number15/18
Codon_changeggA/ggT
Amino_acid_changeG
T08A11.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT08A11.1b.1:c.4200A>T
HGVSpCE54613:p.Gly1400=
cDNA_position4296
CDS_position4200
Protein_position1400
Exon_number16/19
Codon_changeggA/ggT
Amino_acid_changeG
T08A11.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT08A11.1a.1:c.4194A>T
HGVSpCE54207:p.Gly1398=
cDNA_position4294
CDS_position4194
Protein_position1398
Exon_number16/19
Codon_changeggA/ggT
Amino_acid_changeG
ReferenceWBPaper00037807
MethodWGS_De_Bono