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WormBase Tree Display for Variation: WBVar00092272

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Name Class

WBVar00092272NamePublic_nameok1001
Other_nameZK899.8b.1:c.353-3113_353-1610delinsAA
ZK899.8d.1:c.254-3113_254-1610delinsAA
ZK899.8a.1:c.524-3113_524-1610delinsAA
ZK899.8e.1:c.47-3113_47-1610delinsAA
ZK899.8i.2:c.-680-3113_-680-1610delinsAA
ZK899.8c.1:c.620-3113_620-1610delinsAA
ZK899.8i.3:c.-681+2333_-680-1610delinsAA
ZK899.8k.1:c.524-3113_524-1610delinsAA
HGVSgCHROMOSOME_X:g.9493428_9494931delinsAA
Sequence_detailsSMapS_parentSequenceT19C11
Flanking_sequencesaattttatgatactcatttgtgaattttggtatacaggagagtgggcggagtgacagaga
Mapping_targetT19C11
Type_of_mutationInsertionAA
Deletion
PCR_productok1001_external
ok1001_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00035972
LaboratoryRB
PersonWBPerson46
KO_consortium_allele
StatusLive
AffectsGeneWBGene00001516
TranscriptZK899.8a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK899.8a.1:c.524-3113_524-1610delinsAA
Intron_number4/19
ZK899.8i.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK899.8i.2:c.-680-3113_-680-1610delinsAA
Intron_number1/18
ZK899.8e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK899.8e.1:c.47-3113_47-1610delinsAA
Intron_number2/16
ZK899.8c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK899.8c.1:c.620-3113_620-1610delinsAA
Intron_number2/17
ZK899.8b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK899.8b.1:c.353-3113_353-1610delinsAA
Intron_number3/19
ZK899.8i.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK899.8i.3:c.-681+2333_-680-1610delinsAA
Intron_number1/18
ZK899.8d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK899.8d.1:c.254-3113_254-1610delinsAA
Intron_number1/16
ZK899.8k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK899.8k.1:c.524-3113_524-1610delinsAA
Intron_number4/19
IsolationMutagenUV/TMP
RemarkSequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele