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WormBase Tree Display for Variation: WBVar01979988

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Name Class

WBVar01979988NamePublic_nameWBVar01979988
Other_namecewivar00706065
Y41G9A.4c.1:c.1569+56_1569+57insT
Y41G9A.4b.1:c.1569+56_1569+57insT
Y41G9A.4a.1:c.*35_*36insT
Y41G9A.4d.1:c.1569+56_1569+57insT
HGVSgCHROMOSOME_X:g.2961670_2961671insT
Sequence_detailsSMapS_parentSequenceY41G9A
Flanking_sequencesTTAGATTTTAGTGGGCGACAAAAATCATAGTTTTTTTTTAATATAAAAAACTCTCGGCGA
Mapping_targetY41G9A
Source_location225CHROMOSOME_X29616602961661From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021528
TranscriptY41G9A.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4c.1:c.1569+56_1569+57insT
Intron_number12/20
Y41G9A.4a.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScY41G9A.4a.1:c.*35_*36insT
cDNA_position1625-1626
Exon_number12/12
Y41G9A.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4d.1:c.1569+56_1569+57insT
Intron_number11/19
Y41G9A.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4b.1:c.1569+56_1569+57insT
Intron_number12/21
MethodWGS_Flibotte