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: WBVar01814064

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01814064NamePublic_nameWBVar01814064
Other_namecewivar00525341
F56B6.2i.1:c.1702+506T>C
F56B6.2h.1:c.1711+506T>C
F56B6.2e.1:c.211+506T>C
F56B6.2a.1:c.1696+506T>C
F56B6.2c.1:c.511+506T>C
F56B6.2b.1:c.1585+506T>C
F56B6.2j.1:c.1705+506T>C
HGVSgCHROMOSOME_X:g.3550777T>C
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesACACTCATTTCCAACTGATTTTATGTGAAATCCAGGAAAGGAACTTTTAATACTGATTGG
Mapping_targetF56B6
Source_location225CHROMOSOME_X35507643550764From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.1705+506T>C
Intron_number9/14
F56B6.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2e.1:c.211+506T>C
Intron_number1/7
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.1702+506T>C
Intron_number10/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.1585+506T>C
Intron_number9/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.1696+506T>C
Intron_number10/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.1711+506T>C
Intron_number10/16
F56B6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2c.1:c.511+506T>C
Intron_number4/9
MethodWGS_Flibotte