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WormBase Tree Display for Variation: WBVar00076778

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Name Class

WBVar00076778EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar00076778
Other_namehaw101138
cewivar00271368
C33D12.2b.2:c.-9-534C>T
C33D12.2b.4:c.-9-534C>T
C33D12.2b.3:c.-9-534C>T
C33D12.2a.1:c.1633-534C>T
C33D12.2b.5:c.-9-534C>T
C33D12.2b.1:c.-9-534C>T
C33D12.2b.6:c.-9-534C>T
C33D12.2c.1:c.1633-534C>T
HGVSgCHROMOSOME_X:g.3039559G>A
Sequence_detailsSMapS_parentSequenceM02F4
Flanking_sequencesttgtagtttttttctagaattctgataaaaattttggagaatttctaaat
Mapping_targetM02F4
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisWGS_Hawaiian_Waterston
Million_mutation_project_reanalysis
WGS_Andersen
LaboratoryRW
QX
PersonWBPerson1562
WBPerson1730
AnalysisWGS_Hawaiian_Waterston
Million_mutation_project_reanalysis
WGS_Andersen
HistoryAcquires_mergeWBVar01468145
StatusLive
AffectsGeneWBGene00016343
TranscriptC33D12.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33D12.2c.1:c.1633-534C>T
Intron_number9/15
C33D12.2b.4VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33D12.2b.4:c.-9-534C>T
Intron_number8/14
C33D12.2b.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33D12.2b.3:c.-9-534C>T
Intron_number7/13
C33D12.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33D12.2a.1:c.1633-534C>T
Intron_number10/15
C33D12.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33D12.2b.1:c.-9-534C>T
Intron_number9/15
C33D12.2b.6VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33D12.2b.6:c.-9-534C>T
Intron_number1/7
C33D12.2b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33D12.2b.2:c.-9-534C>T
Intron_number7/13
C33D12.2b.5VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33D12.2b.5:c.-9-534C>T
Intron_number2/8
ReferenceWBPaper00040707
Remark[20081124 db] this Variation was previously named hw101138
MethodWGS_Hawaiian_Waterston