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WormBase Tree Display for Variation: WBVar01972512

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Name Class

WBVar01972512NamePublic_nameWBVar01972512
Other_namecewivar00698489
T27C4.4b.1:c.2607+30_2607+31insTT
T27C4.4b.2:c.2607+30_2607+31insTT
T27C4.4a.1:c.2607+30_2607+31insTT
T27C4.4e.1:c.2202+30_2202+31insTT
T27C4.4d.1:c.*24_*25insTT
HGVSgCHROMOSOME_V:g.3710148_3710149insTT
Sequence_detailsSMapS_parentSequenceT27C4
Flanking_sequencesGTATGAGCGAGCGAGTTTGTGAGGATGCTGTTTTTTTTTCGATTTTTGCAAAACATTTAA
Mapping_targetT27C4
Source_location225CHROMOSOME_V37101353710136From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionTT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003025
TranscriptT27C4.4d.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScT27C4.4d.1:c.*24_*25insTT
cDNA_position2661-2662
Exon_number8/9
T27C4.4b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4b.2:c.2607+30_2607+31insTT
Intron_number7/8
T27C4.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4a.1:c.2607+30_2607+31insTT
Intron_number7/9
T27C4.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4e.1:c.2202+30_2202+31insTT
Intron_number4/4
T27C4.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4b.1:c.2607+30_2607+31insTT
Intron_number7/8
MethodWGS_Flibotte