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WormBase Tree Display for Variation: WBVar00059055

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Name Class

WBVar00059055EvidencePaper_evidenceWBPaper00004703
NamePublic_nameWBVar00059055
Other_name (12)
HGVSgCHROMOSOME_X:g.9093651C>T
Sequence_detailsSMapS_parentSequenceH08J11
Flanking_sequencesacggtgcttttttgcattgattttggtgtttttactccatttcattttaactatcgcttgttcaaactcccgttttcttccatccggattttttattgatgcatcttgtaatccatcgctcaaaatgcaaaaaaaatcaatgaaaacgatatgggtgatgattatattgtttggtcacgaacagttatgcaaatcgactatgatggttcccaccatcccgtcccccgtcctttccgcttcactccgttttctcgtttgtctttttctttttgatggcctcgcaccatcaaaattatgtggtttgagcatttgagcatttacactggttaaaatatttttgagagccaattgccaaatcattcgaaaaacccaatatgaaaacatttttctgaatttttaaaaataaggtgaaagatagaacgtacaacatgagtacaatttgggcaatatcctgttgccatgaaattagaatgttttcattcaaataatattaagaggtcaaataaaattttcgtttgcttgatttagtttgaaaattggtctctaatttattttgaaagtttgctaagaaatttaacaaacttgccgtttttgtaaacg
Mapping_targetH08J11
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (38)
LaboratoryRW
PersonWBPerson6900
WBPerson1562
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
SNP_Wicks
WGS_Hawaiian_Waterston
HistoryAcquires_mergeWBVar00081763
WBVar00245317
StatusLive
AffectsGeneWBGene00000100
TranscriptC25A11.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4d.1:c.1071+1079C>T
Intron_number8/29
C25A11.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4a.1:c.-205+1079C>T
Intron_number7/30
C25A11.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4f.1:c.1071+1079C>T
Intron_number7/28
C25A11.4a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4a.3:c.-205+1079C>T
Intron_number2/25
C25A11.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4c.1:c.1071+1079C>T
Intron_number8/23
C25A11.4k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4k.1:c.288+1079C>T
Intron_number1/22
C25A11.4a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4a.2:c.-205+1079C>T
Intron_number3/26
C25A11.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4b.1:c.1071+1079C>T
Intron_number7/18
ReferenceWBPaper00004703
MethodWGS_Pasadena_Quinlan