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WormBase Tree Display for Variation: WBVar01456849

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Name Class

WBVar01456849EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01456849
Other_namecewivar00552987
Y51H4A.25e.1:c.1236+6C>A
Y51H4A.25a.1:c.1086+6C>A
HGVSgCHROMOSOME_IV:g.16742200C>A
Sequence_detailsSMapS_parentSequenceY43D4A
Flanking_sequencesATTCATCAACCAGTTTGATCGAACGGTATCATAAAAACTAGAAAACGTTTCTAAAAGTTT
Mapping_targetY43D4A
Type_of_mutationSubstitutionca
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022928From_analysisWGS_Andersen
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00023144From_analysisWGS_Andersen
WBStrain00023149From_analysisWGS_Andersen
WBStrain00023150From_analysisWGS_Andersen
WBStrain00023151From_analysisWGS_Andersen
WBStrain00023211From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193342506
dbSNP_ssss295518425
StatusLive
AffectsGeneWBGene00013119
TranscriptY51H4A.25a.1VEP_consequencesplice_region_variant,intron_variant
VEP_impactLOW
HGVScY51H4A.25a.1:c.1086+6C>A
Intron_number6/10
Y51H4A.25e.1VEP_consequencesplice_region_variant,intron_variant
VEP_impactLOW
HGVScY51H4A.25e.1:c.1236+6C>A
Intron_number7/11
ReferenceWBPaper00040707
MethodWGS_Andersen