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WormBase Tree Display for Variation: WBVar00172968

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Name Class

WBVar00172968NamePublic_nameWBVar00172968
Other_name (14)
HGVSgCHROMOSOME_II:g.6930673C>T
Sequence_detailsSMapS_parentSequenceF22D3
Flanking_sequencescatcattaggaccatctacaagtagtcacctccaggaataatagttcctt
Mapping_targetF22D3
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00004602From_analysisWGS_De_Bono
WGS_Hawaiian_Waterston
WGS_Yanai
Million_mutation_project_reanalysis
WBStrain00004604From_analysisWGS_Pasadena_Quinlan
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryRW
AX
PersonWBPerson1562
WBPerson6900
WBPerson4037
AnalysisWGS_Hawaiian_Waterston
WGS_De_Bono
WGS_Yanai
Million_mutation_project_reanalysis
WGS_Pasadena_Quinlan
HistoryAcquires_mergeWBVar00225266
WBVar00551124
WBVar01372957
StatusLive
AffectsGeneWBGene00017699
TranscriptF22D3.2g.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF22D3.2g.1:c.141C>T
HGVSpCE48418:p.Ser47=
cDNA_position238
CDS_position141
Protein_position47
Exon_number4/19
Codon_changeagC/agT
Amino_acid_changeS
F22D3.2e.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF22D3.2e.1:c.141C>T
HGVSpCE48451:p.Ser47=
cDNA_position238
CDS_position141
Protein_position47
Exon_number4/19
Codon_changeagC/agT
Amino_acid_changeS
F22D3.2d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF22D3.2d.1:c.141C>T
HGVSpCE47786:p.Ser47=
cDNA_position238
CDS_position141
Protein_position47
Exon_number4/19
Codon_changeagC/agT
Amino_acid_changeS
F22D3.2f.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF22D3.2f.1:c.141C>T
HGVSpCE48472:p.Ser47=
cDNA_position141
CDS_position141
Protein_position47
Exon_number2/11
Codon_changeagC/agT
Amino_acid_changeS
F22D3.2j.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF22D3.2j.1:c.141C>T
HGVSpCE51723:p.Ser47=
cDNA_position245
CDS_position141
Protein_position47
Exon_number4/19
Codon_changeagC/agT
Amino_acid_changeS
ReferenceWBPaper00038208
WBPaper00037807
Remark[20081124 db] this Variation was previously named hw26218
MethodWGS_Hawaiian_Waterston