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WormBase Tree Display for Variation: WBVar00093898

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Name Class

WBVar00093898NamePublic_nameok2801
Other_nameCE28614:p.Asp70ValfsTer5
M01H9.3a.1:c.204_714del
M01H9.3c.1:c.51_561del
M01H9.3d.2:c.21_531del
CE40982:p.Asp9ValfsTer5
M01H9.3b.2:c.18+3_432del
M01H9.3b.1:c.18+3_432del
M01H9.3d.1:c.21_531del
CE37722:p.Asp19ValfsTer5
M01H9.3e.1:c.18+3_426del
HGVSgCHROMOSOME_IV:g.4468945_4469821del
Sequence_detailsSMapS_parentSequenceM01H9
Flanking_sequencestattcagtctttcatgtagttgctacgcttacttgtggagccttggacatcctgaaatat
Mapping_targetM01H9
Type_of_mutationDeletion
PCR_productok2801_external
ok2801_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00032799
LaboratoryRB
PersonWBPerson46
KO_consortium_allele
StatusLive
AffectsGeneWBGene00019719
TranscriptM01H9.3b.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScM01H9.3b.2:c.18+3_432del
cDNA_position?-649
CDS_position?-432
Protein_position?-144
Intron_number2-4/5
Exon_number3-5/6
M01H9.3a.1 (11)
M01H9.3e.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScM01H9.3e.1:c.18+3_426del
cDNA_position?-1411
CDS_position?-426
Protein_position?-142
Intron_number2-4/5
Exon_number3-5/6
M01H9.3d.2 (11)
M01H9.3c.1 (11)
M01H9.3d.1 (11)
M01H9.3b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScM01H9.3b.1:c.18+3_432del
cDNA_position?-545
CDS_position?-432
Protein_position?-144
Intron_number3-5/6
Exon_number4-6/7
IsolationMutagenEMS
RemarkSequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele