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WormBase Tree Display for Variation: WBVar00275065

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Name Class

WBVar00275065EvidencePaper_evidenceWBPaper00024480
NamePublic_namevs19
HGVSgCHROMOSOME_II:g.6109478_6111040del
Sequence_detailsSMapS_parentSequenceC29H12
Flanking_sequencesgagttcaggtaatcatttttagtgataaatgattaatattatattcttgtttttttctag
Mapping_targetC29H12
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00026361
LaboratoryLX
StatusLive
AffectsGeneWBGene00016236
WBGene00004346
TranscriptC29H12.3a.2VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number5/6
Exon_number6-7/7
C29H12.3c.3VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number3/4
Exon_number4-5/5
C29H12.5.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number9-10/11
Exon_number10-12/12
C29H12.3b.2VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number4/5
Exon_number5-6/6
C29H12.3c.1VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number4/5
Exon_number5-6/6
C29H12.3a.1VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number6/7
Exon_number7-8/8
C29H12.3c.2VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number4/5
Exon_number5-6/6
C29H12.3b.1VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number5/6
Exon_number6-7/7
InteractorWBInteraction000569525
WBInteraction000569527
GeneticsInterpolated_map_positionII-0.475258
Mapping_dataIn_multi_point4907
DescriptionPhenotype (9)
Phenotype_not_observedWBPhenotype:0002535Paper_evidenceWBPaper00028963
Curator_confirmedWBPerson48
Remarkbased on dye fillingPaper_evidenceWBPaper00028963
Curator_confirmedWBPerson48
RecessivePaper_evidenceWBPaper00028963
Curator_confirmedWBPerson48
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00028963
Curator_confirmedWBPerson48
ReferenceWBPaper00031936
WBPaper00028963
WBPaper00048845
WBPaper00043948
Remarkvs19 is a 1563 bp mutation
MethodDeletion_allele