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WormBase Tree Display for Variation: WBVar01134589

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Name Class

WBVar01134589NamePublic_namegk493893
Other_nameF56B6.2i.1:c.1492-288G>A
F56B6.2b.1:c.1375-288G>A
F56B6.2c.1:c.301-288G>A
F56B6.2a.1:c.1486-288G>A
F56B6.2j.1:c.1495-288G>A
F56B6.2h.1:c.1501-288G>A
HGVSgCHROMOSOME_X:g.3549773G>A
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesTGTACTCTGTGCCTATACCGTTGACATTGATTATTTATCAAGTATTTTCATTTTCAGTTCTCAACGCGTATTGATCAGTTTCATTGCAATTTGTAACTTT
Mapping_targetF56B6
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00039150
LaboratoryVC
AnalysisMillion_Mutation_Project
StatusLive
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.1495-288G>A
Intron_number8/14
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.1492-288G>A
Intron_number9/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.1375-288G>A
Intron_number8/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.1486-288G>A
Intron_number9/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.1501-288G>A
Intron_number9/16
F56B6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2c.1:c.301-288G>A
Intron_number3/9
ReferenceWBPaper00042537
MethodMillion_mutation