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: WBVar00143023

expand all nodes | collapse all nodes | view schema

Name Class

WBVar00143023EvidencePerson_evidenceWBPerson499
NamePublic_namee189
Other_nameZK637.8a.1:c.614+288G>A
ZK637.8e.1:c.460-345G>A
ZK637.8f.1:c.460-1G>A
ZK637.8c.1:c.460-345G>A
ZK637.8b.1:c.460-1G>A
ZK637.8d.1:c.614+288G>A
HGVSgCHROMOSOME_III:g.8906966G>A
Sequence_detailsSMapS_parentSequenceZK637
Flanking_sequencestaaaatctccttcactaacacagccgggactggagaaatgttgcca
Mapping_targetZK637
Type_of_mutationSubstitutionga
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
Strain (303)
LaboratoryCB
OJ
StatusLive
AffectsGeneWBGene00006768
TranscriptZK637.8c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK637.8c.1:c.460-345G>A
Intron_number4/11
ZK637.8f.1VEP_consequencesplice_acceptor_variant
VEP_impactHIGH
HGVScZK637.8f.1:c.460-1G>A
Intron_number4/11
ZK637.8e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK637.8e.1:c.460-345G>A
Intron_number4/11
ZK637.8d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK637.8d.1:c.614+288G>A
Intron_number5/11
ZK637.8b.1VEP_consequencesplice_acceptor_variant
VEP_impactHIGH
HGVScZK637.8b.1:c.460-1G>A
Intron_number4/11
ZK637.8a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK637.8a.1:c.614+288G>A
Intron_number5/11
InteractorWBInteraction000524785
IsolationMutagenEMS
GeneticsInterpolated_map_positionIII-0.00184685
Mapping_dataIn_2_point (31)
In_multi_point64
65
66
68
70
71
76
77
78
79
80
86
87
90
93
218
219
220
315
325
326
347
356
384
385
386
387
388
404
405
406
407
408
412
428
430
488
491
492
498
502
506
513
530
580
581
584
585
588
589
611
613
629
630
642
729
746
753
758
759
761
855
863
864
868
870
887
888
889
890
892
894
895
1080
1085
1086
1112
1255
1357
1363
1364
1401
1402
1412
1414
1421
1489
1490
1497
1498
1500
1501
1503
1506
1510
1577
1637
1669
1726
1728
1729
1730
1731
1735
1752
1754
1816
1836
1863
2012
2018
2055
2057
2074
2099
2101
2151
2179
2185
2190
2198
2199
2223
2226
2235
2246
2305
2306
2312
2425
2462
2463
2740
2742
2744
2755
2764
2766
3014
3138
3155
3156
3166
3177
3178
3225
3246
3261
3297
3298
3299
3300
3301
3302
3324
3325
3326
3327
3328
3329
3330
3331
3332
3333
3334
3335
3336
3337
3338
3339
3340
In_pos_neg_data806
3726
DescriptionPhenotype (26)
Phenotype_not_observedWBPhenotype:0001426Paper_evidenceWBPaper00004883
Curator_confirmedWBPerson712
Phenotype_assayGenotypearIs37Paper_evidenceWBPaper00004883
Curator_confirmedWBPerson712
WBPhenotype:0001645Paper_evidenceWBPaper00040284
Curator_confirmedWBPerson2987
RemarkTable 1Paper_evidenceWBPaper00040284
Curator_confirmedWBPerson2987
Reference (32)
RemarkVariation stub/paper connection generated from the May 2021 NN VFP dataset.
Created by WBPerson51134 from the NN_VFP_triage_pipeline
MethodSubstitution_allele