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: WBVar00499333

expand all nodes | collapse all nodes | view schema

Name Class

WBVar00499333NamePublic_namegk276090
Other_nameF56B6.2b.1:c.1374+689G>A
F56B6.2j.1:c.1494+689G>A
F56B6.2i.1:c.1491+689G>A
F56B6.2a.1:c.1485+689G>A
F56B6.2h.1:c.1500+689G>A
F56B6.2c.1:c.300+689G>A
HGVSgCHROMOSOME_X:g.3548608G>A
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesGAAAACTGATTTCCCTCAATTTTTAATTCGAAATGAAAAAATTTCCAAAATTTTGAAGAAATTTTATTTTGATTTTTGGTCACTTTTGAATCATAGTTTT
Mapping_targetF56B6
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00038047
LaboratoryVC
AnalysisMillion_Mutation_Project
StatusLive
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.1494+689G>A
Intron_number8/14
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.1491+689G>A
Intron_number9/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.1374+689G>A
Intron_number8/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.1485+689G>A
Intron_number9/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.1500+689G>A
Intron_number9/16
F56B6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2c.1:c.300+689G>A
Intron_number3/9
ReferenceWBPaper00042537
MethodMillion_mutation