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WormBase Tree Display for Variation: WBVar01471761

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Name Class

WBVar01471761EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01471761
Other_namecewivar00542946
CE03262:p.Gly227=
F16H9.2b.1:c.35-41207A>T
F16H9.2a.1:c.-23-41207A>T
F22E10.3.1:c.681A>T
HGVSgCHROMOSOME_X:g.12748510T>A
Sequence_detailsSMapS_parentSequenceF22E10
Flanking_sequencesGATAAGCATAGCAAATCCTCTGAGGAGCACCCAAGCTTATCTCCGATACCTTCACGAATT
Mapping_targetF22E10
Type_of_mutationSubstitutionta
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006690From_analysisWGS_Andersen
WBStrain00006691From_analysisWGS_Andersen
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00022888From_analysisWGS_Andersen
WBStrain00022889From_analysisWGS_Andersen
WBStrain00022894From_analysisWGS_Andersen
WBStrain00023065From_analysisWGS_Andersen
WBStrain00023085From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193357063
dbSNP_ssss295532982
StatusLive
AffectsGeneWBGene00004008
WBGene00008901
TranscriptF16H9.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.2b.1:c.35-41207A>T
Intron_number1/3
F16H9.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.2a.1:c.-23-41207A>T
Intron_number1/4
F22E10.3.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF22E10.3.1:c.681A>T
HGVSpCE03262:p.Gly227=
cDNA_position706
CDS_position681
Protein_position227
Exon_number5/10
Codon_changeggA/ggT
Amino_acid_changeG
ReferenceWBPaper00040707
MethodWGS_Andersen