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WormBase Tree Display for Variation: WBVar00092380

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Name Class

WBVar00092380NamePublic_nameok1112
Other_nameF54E4.1b.1:c.3884+12_4975-1delinsAAAA
F54E4.1d.1:c.3857+12_4948-1delinsAAAA
F54E4.1c.1:c.3857+12_4948-1delinsAAAA
F54E4.1f.1:c.3890+12_4981-1delinsAAAA
F54E4.1a.1:c.3884+12_4975-1delinsAAAA
F54E4.1h.1:c.3851+12_4942-1delinsAAAA
F54E4.1e.1:c.3890+12_4981-1delinsAAAA
F54E4.1g.1:c.3851+12_4942-1delinsAAAA
HGVSgCHROMOSOME_X:g.14616668_14618088delinsAAAA
Sequence_detailsSMapS_parentSequenceF54E4
Flanking_sequencesttgtgagcacaatgaacaagtaagccacacattgcaaaagctgcattccagcaaaatcaa
Mapping_targetF54E4
Type_of_mutationInsertionAAAA
Deletion
PCR_productok1112_external
ok1112_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00036076
LaboratoryRB
PersonWBPerson46
KO_consortium_allele
StatusLive
AffectsGeneWBGene00004313
TranscriptF54E4.1a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF54E4.1a.1:c.3884+12_4975-1delinsAAAA
Intron_number17-20/33
Exon_number18-20/34
F54E4.1g.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF54E4.1g.1:c.3851+12_4942-1delinsAAAA
Intron_number17-20/34
Exon_number18-20/35
F54E4.1e.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF54E4.1e.1:c.3890+12_4981-1delinsAAAA
Intron_number16-19/32
Exon_number17-19/33
F54E4.1d.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF54E4.1d.1:c.3857+12_4948-1delinsAAAA
Intron_number16-19/31
Exon_number17-19/32
F54E4.1f.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF54E4.1f.1:c.3890+12_4981-1delinsAAAA
Intron_number16-19/31
Exon_number17-19/32
F54E4.1c.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF54E4.1c.1:c.3857+12_4948-1delinsAAAA
Intron_number16-19/32
Exon_number17-19/33
F54E4.1h.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF54E4.1h.1:c.3851+12_4942-1delinsAAAA
Intron_number17-20/33
Exon_number18-20/34
F54E4.1b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF54E4.1b.1:c.3884+12_4975-1delinsAAAA
Intron_number16-19/33
Exon_number17-19/34
IsolationMutagenUV/TMP
GeneticsMapping_dataIn_multi_point5182
RemarkSequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele