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WormBase Tree Display for Variation: WBVar00142975

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Name Class

WBVar00142975EvidencePaper_evidenceWBPaper00003757
NamePublic_namee120
Other_nameF26C11.2.1:c.597+1G>A
HGVSgCHROMOSOME_II:g.9898071C>T
Sequence_detailsSMapS_parentSequenceF26C11
Flanking_sequencescgaccaaatgcgaaatatcccagggttcagtaatttgtttcgtatagtttttcgacaaatt
Mapping_targetF26C11
Type_of_mutationSubstitutionga
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
Strain (254)
LaboratoryCB
StatusLive
AffectsGeneWBGene00006744
TranscriptF26C11.2.1VEP_consequencesplice_donor_variant
VEP_impactHIGH
HGVScF26C11.2.1:c.597+1G>A
Intron_number6/7
Interactor (16)
GeneticsInterpolated_map_positionII1.76951
Mapping_dataIn_2_point (49)
In_multi_point (159)
In_pos_neg_data (22)
Marked_rearrangementmIn1[unc-4(e120) dpy-10(e128)]
mIn1[unc-4(e120)]
DescriptionPhenotype (24)
Phenotype_not_observedWBPhenotype:0000641Person_evidenceWBPerson261
Curator_confirmedWBPerson712
RemarkHealthy, active.Person_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0001426Paper_evidenceWBPaper00004883
Curator_confirmedWBPerson712
Phenotype_assayGenotypearIs37Paper_evidenceWBPaper00004883
Curator_confirmedWBPerson712
WBPhenotype:0001645Paper_evidenceWBPaper00040284
Curator_confirmedWBPerson2987
RemarkTable S2Paper_evidenceWBPaper00040284
Curator_confirmedWBPerson2987
ReferenceWBPaper00001502
WBPaper00039982
WBPaper00040284
WBPaper00040262
WBPaper00043908
WBPaper00029020
WBPaper00000031
WBPaper00010445
WBPaper00022514
WBPaper00023402
WBPaper00004883
WBPaper00012694
WBPaper00011060
WBPaper00003998
WBPaper00015132
WBPaper00020813
WBPaper00014501
WBPaper00014296
WBPaper00016533
WBPaper00014440
WBPaper00016150
WBPaper00015940
WBPaper00015529
WBPaper00015530
WBPaper00013780
WBPaper00016593
WBPaper00014830
WBPaper00011765
WBPaper00022498
WBPaper00024161
WBPaper00012591
WBPaper00015277
WBPaper00011777
WBPaper00022296
WBPaper00016421
WBPaper00013923
WBPaper00014042
WBPaper00014181
WBPaper00016535
WBPaper00014111
WBPaper00022197
WBPaper00018570
WBPaper00016685
WBPaper00017118
WBPaper00016532
WBPaper00015263
WBPaper00016423
WBPaper00016548
WBPaper00016399
WBPaper00019566
WBPaper00015881
WBPaper00001826
WBPaper00061034
WBPaper00061175
RemarkManually curated Gene associations preserved as a text remark so that VEP is the canonical predictor of consequence: WBGene00006744 Donor
Variation stub/paper connection generated from the May 2021 NN VFP dataset.
Created by WBPerson51134 from the NN_VFP_triage_pipeline
MethodSubstitution_allele