WormBase Tree Display for Variation: WBVar00093610
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WBVar00093610 | Name | Public_name | ok2464 | ||
---|---|---|---|---|---|
Other_name | F17C11.9b.3:c.512-145_723del | ||||
F17C11.9c.1:c.488-145_699del | |||||
F17C11.9b.2:c.512-145_723del | |||||
F17C11.9b.1:c.512-145_723del | |||||
F17C11.9a.1:c.587-145_798del | |||||
HGVSg | CHROMOSOME_V:g.10966844_10967200del | ||||
Sequence_details | SMap | S_parent | Sequence | F17C11 | |
Flanking_sequences | aacgtttttcatgggactgagagttggaaa | accaaggctatcccacacttctgggagaac | |||
Mapping_target | F17C11 | ||||
Type_of_mutation | Deletion | ||||
PCR_product | ok2464_external | ||||
ok2464_internal | |||||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00036929 | ||||
Laboratory | RB | ||||
Person | WBPerson46 | ||||
KO_consortium_allele | |||||
Status | Live | ||||
Affects | Gene | WBGene00045367 | |||
WBGene00008920 | |||||
Transcript | F17C11.9b.1 | VEP_consequence | splice_acceptor_variant,coding_sequence_variant,intron_variant | ||
VEP_impact | HIGH | ||||
HGVSc | F17C11.9b.1:c.512-145_723del | ||||
cDNA_position | ?-872 | ||||
CDS_position | ?-723 | ||||
Protein_position | ?-241 | ||||
Intron_number | 5/7 | ||||
Exon_number | 6/8 | ||||
F17C11.9b.3 | VEP_consequence | splice_acceptor_variant,coding_sequence_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | F17C11.9b.3:c.512-145_723del | ||||
cDNA_position | ?-813 | ||||
CDS_position | ?-723 | ||||
Protein_position | ?-241 | ||||
Intron_number | 4/6 | ||||
Exon_number | 5/7 | ||||
F17C11.9c.1 | VEP_consequence | splice_acceptor_variant,coding_sequence_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | F17C11.9c.1:c.488-145_699del | ||||
cDNA_position | ?-699 | ||||
CDS_position | ?-699 | ||||
Protein_position | ?-233 | ||||
Intron_number | 4/5 | ||||
Exon_number | 5/6 | ||||
F17C11.15 | VEP_consequence | non_coding_transcript_exon_variant | |||
VEP_impact | MODIFIER | ||||
cDNA_position | 147-? | ||||
Exon_number | 1/1 | ||||
F17C11.9a.1 | VEP_consequence | splice_acceptor_variant,coding_sequence_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | F17C11.9a.1:c.587-145_798del | ||||
cDNA_position | ?-904 | ||||
CDS_position | ?-798 | ||||
Protein_position | ?-266 | ||||
Intron_number | 5/7 | ||||
Exon_number | 6/8 | ||||
F17C11.9b.2 | VEP_consequence | splice_acceptor_variant,coding_sequence_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | F17C11.9b.2:c.512-145_723del | ||||
cDNA_position | ?-841 | ||||
CDS_position | ?-723 | ||||
Protein_position | ?-241 | ||||
Intron_number | 5/7 | ||||
Exon_number | 6/8 | ||||
Isolation | Mutagen | UV/TMP | |||
Remark | Sequenced by the C. elegans Gene Knockout Consortium | Paper_evidence | WBPaper00041807 | ||
Method | KO_consortium_allele |