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WormBase Tree Display for Variation: WBVar02039447

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Name Class

WBVar02039447NamePublic_nameWBVar02039447
Other_namecewivar00768189
C32E8.10a.1:c.765+21dup
C32E8.10c.1:c.765+21dup
C32E8.10e.1:c.765+21dup
C32E8.10d.1:c.765+21dup
C32E8.10h.1:c.765+21dup
C32E8.10b.1:c.765+21dup
HGVSgCHROMOSOME_I:g.3803994_3803995insA
Sequence_detailsSMapS_parentSequenceC32E8
Flanking_sequencesTTTCAAAGACCTCTTTTTTTTTTTAAATTGAAAAAAAAAGTATTTTTTTACCTTATAAGT
Mapping_targetC32E8
Source_location225CHROMOSOME_I38039973803998From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006751
TranscriptC32E8.10d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC32E8.10d.1:c.765+21dup
Intron_number5/11
C32E8.10b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC32E8.10b.1:c.765+21dup
Intron_number5/9
C32E8.10e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC32E8.10e.1:c.765+21dup
Intron_number5/10
C32E8.10c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC32E8.10c.1:c.765+21dup
Intron_number5/11
C32E8.10h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC32E8.10h.1:c.765+21dup
Intron_number5/9
C32E8.10a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC32E8.10a.1:c.765+21dup
Intron_number5/10
MethodWGS_Flibotte