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WormBase Tree Display for Variation: WBVar01447470

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Name Class

WBVar01447470EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01447470
Other_nameK01B6.1.3:c.396A>G
CE00238:p.Gln132=
K01B6.1.2:c.396A>G
K01B6.1.1:c.396A>G
HGVSgCHROMOSOME_III:g.9293893A>G
Sequence_detailsSMapS_parentSequenceK01B6
Flanking_sequencesACAGCAGCAACAAAATCAGAATCCGAGTCAAGTCAGTCTTCTTCCAGTGACCGTAAGAGG
Mapping_targetK01B6
Type_of_mutationSubstitutionag
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00031279From_analysisWGS_Andersen
WBStrain00031284From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193333939
dbSNP_ssss295509858
StatusLive
AffectsGeneWBGene00010453
TranscriptK01B6.1.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScK01B6.1.1:c.396A>G
HGVSpCE00238:p.Gln132=
cDNA_position559
CDS_position396
Protein_position132
Exon_number4/10
Codon_changecaA/caG
Amino_acid_changeQ
K01B6.1.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScK01B6.1.2:c.396A>G
HGVSpCE00238:p.Gln132=
cDNA_position609
CDS_position396
Protein_position132
Exon_number5/11
Codon_changecaA/caG
Amino_acid_changeQ
K01B6.1.3VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScK01B6.1.3:c.396A>G
HGVSpCE00238:p.Gln132=
cDNA_position613
CDS_position396
Protein_position132
Exon_number5/11
Codon_changecaA/caG
Amino_acid_changeQ
ReferenceWBPaper00040707
MethodWGS_Andersen