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: WBVar01830094

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01830094NamePublic_nameWBVar01830094
Other_namecewivar00542200
F56B6.2j.1:c.1946+813C>G
F56B6.2i.1:c.1943+813C>G
F56B6.2e.1:c.452+813C>G
F56B6.2a.1:c.1937+813C>G
F56B6.2c.1:c.752+813C>G
F56B6.2b.1:c.1826+813C>G
F56B6.2h.1:c.1952+813C>G
HGVSgCHROMOSOME_X:g.3553739C>G
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesTCGGAATTTTTTGGCAATTCAGCAGTTCGGAACAGTAGTCCAAATTATGGGTAACTGCCA
Mapping_targetF56B6
Source_location225CHROMOSOME_X35537263553726From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022886From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.1946+813C>G
Intron_number11/14
F56B6.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2e.1:c.452+813C>G
Intron_number3/7
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.1943+813C>G
Intron_number12/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.1826+813C>G
Intron_number11/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.1937+813C>G
Intron_number12/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.1952+813C>G
Intron_number12/16
F56B6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2c.1:c.752+813C>G
Intron_number6/9
MethodWGS_Flibotte