Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01759446

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01759446NamePublic_nameWBVar01759446
Other_namecewivar00459183
F38B2.1d.1:c.145+18T>C
F38B2.1e.1:c.181+18T>C
F38B2.1c.1:c.70+18T>C
F38B2.1b.1:c.94+18T>C
F38B2.1a.1:c.94+18T>C
HGVSgCHROMOSOME_X:g.11273359T>C
Sequence_detailsSMapS_parentSequenceC03A3
Flanking_sequencesGGAAACGTTACTTGTAAGTTTATTGTTGTCGTGCAAAACATTTAAATCAACATATTCCAG
Mapping_targetC03A3
Source_location225CHROMOSOME_X1127329511273295From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00002050
TranscriptF38B2.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF38B2.1b.1:c.94+18T>C
Intron_number3/10
F38B2.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF38B2.1d.1:c.145+18T>C
Intron_number2/8
F38B2.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF38B2.1a.1:c.94+18T>C
Intron_number3/10
F38B2.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF38B2.1e.1:c.181+18T>C
Intron_number2/9
F38B2.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF38B2.1c.1:c.70+18T>C
Intron_number2/9
MethodWGS_Flibotte