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WormBase Tree Display for Variation: WBVar00000007

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Name Class

WBVar00000007EvidenceAuthor_evidenceCurtis L
NamePublic_namead446
HGVSgCHROMOSOME_III:g.5612625_5616891delinsAAAAAA
Sequence_detailsSMapS_parentSequenceC05D2
Flanking_sequencesagactgggcaaaaatctttgacgatctcgaaaatgtggtggtgaaaaaatacaaaataatgaagtaggcacgtgtatgtaggcag
Mapping_targetC05D2
Type_of_mutationInsertionaaaaaa
Deletion
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00027310
WBStrain00027351
LaboratoryDA
StatusLive
AffectsGeneWBGene00015467
WBGene00000239
TranscriptC05D2.4b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position213-?
CDS_position198-?
Protein_position66-?
Intron_number3-8/9
Exon_number3-10/10
C05D2.3.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number2-7/9
Exon_number1-7/10
C05D2.4a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position213-?
CDS_position198-?
Protein_position66-?
Intron_number3-7/8
Exon_number3-9/9
InteractorWBInteraction000500584
IsolationMutagenEMS
Forward_geneticsstandard phenotypic screen
GeneticsInterpolated_map_positionIII-1.46914
Mapping_dataIn_multi_point2312
2693
Description (2)
Disease_infoModels_diseaseDOID:809
DOID:0050742
Models_disease_in_annotationWBDOannot00000679
WBDOannot00000680
ReferenceWBPaper00038382
WBPaper00040570
WBPaper00043908
WBPaper00031936
WBPaper00032335
WBPaper00011911
WBPaper00001861
WBPaper00014504
WBPaper00015782
MethodDeletion_and_insertion_allele