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WormBase Tree Display for Variation: WBVar00088761

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Name Class

WBVar00088761EvidencePaper_evidenceWBPaper00005614
NamePublic_namem889
Other_nameY110A7A.10.1:c.974G>A
CE23248:p.Trp325Ter
HGVSgCHROMOSOME_I:g.5109272G>A
Sequence_detailsSMapS_parentSequenceY110A7A
Flanking_sequencesctcaacttcttgtcgatatggaattgaagtgacaccggcacaatatttgatgtgtggaac
Mapping_targetY110A7A
Type_of_mutationSubstitutiongaPaper_evidenceWBPaper00005614
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006403
LaboratoryDR
StatusLive
AffectsGeneWBGene00000001
TranscriptY110A7A.10.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScY110A7A.10.1:c.974G>A
HGVSpCE23248:p.Trp325Ter
cDNA_position975
CDS_position974
Protein_position325
Exon_number5/7
Codon_changetGg/tAg
Amino_acid_changeW/*
GeneticsInterpolated_map_positionI-0.407165
DescriptionPhenotypeWBPhenotype:0000061Paper_evidenceWBPaper00005729
Curator_confirmedWBPerson1307
RemarkFigure 3IPaper_evidenceWBPaper00005729
Curator_confirmedWBPerson1307
WBPhenotype:0000295Paper_evidenceWBPaper00005729
Curator_confirmedWBPerson1307
RemarkFigure 3JPaper_evidenceWBPaper00005729
Curator_confirmedWBPerson1307
ReferenceWBPaper00005614
WBPaper00005729
RemarkThis substitution is either [g/a] 2nd site mutation or [g/a] 3rd site mutationCurator_confirmedWBPerson2861
MethodSubstitution_allele