WormBase Tree Display for Variation: WBVar00093071
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WBVar00093071 | Name | Public_name | ok1875 | ||
---|---|---|---|---|---|
Other_name | F13D12.7b.3:c.-150_*451del | ||||
F13D12.7b.2:c.-150_*451del | |||||
F13D12.7b.1:c.-150_*451del | |||||
F13D12.7b.4:c.-150_*451del | |||||
F13D12.7a.1:c.412_*451del | |||||
HGVSg | CHROMOSOME_II:g.11743528_11745505del | ||||
Sequence_details | SMap | S_parent | Sequence | F13D12 | |
Flanking_sequences | gtagaatacgatcggggagagaaagagagc | acgagacacccgcacgtttccctcgcgtgt | |||
Mapping_target | F13D12 | ||||
Type_of_mutation | Deletion | ||||
PCR_product | ok1875_external | ||||
ok1875_internal | |||||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00036648 | ||||
Laboratory | RB | ||||
Person | WBPerson46 | ||||
KO_consortium_allele | |||||
Status | Live | ||||
Affects | Gene | WBGene00001679 | |||
Transcript | F13D12.7b.5 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant | ||
VEP_impact | HIGH | ||||
cDNA_position | ?-978 | ||||
Intron_number | 2-4/5 | ||||
Exon_number | 1-6/6 | ||||
F13D12.7a.1 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,stop_lost,3_prime_UTR_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | F13D12.7a.1:c.412_*451del | ||||
cDNA_position | 415-1477 | ||||
CDS_position | 412-? | ||||
Protein_position | 138-? | ||||
Intron_number | 6-9/10 | ||||
Exon_number | 6-11/11 | ||||
F13D12.7b.4 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,start_lost,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | F13D12.7b.4:c.-150_*451del | ||||
cDNA_position | 68-1130 | ||||
Intron_number | 1-5/6 | ||||
Exon_number | 1-7/7 | ||||
F13D12.7b.1 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,start_lost,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | F13D12.7b.1:c.-150_*451del | ||||
cDNA_position | 669-1731 | ||||
Intron_number | 6-10/11 | ||||
Exon_number | 6-12/12 | ||||
F13D12.7b.2 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,start_lost,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | F13D12.7b.2:c.-150_*451del | ||||
cDNA_position | 583-1645 | ||||
Intron_number | 5-9/10 | ||||
Exon_number | 5-11/11 | ||||
F13D12.7b.3 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,start_lost,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | F13D12.7b.3:c.-150_*451del | ||||
cDNA_position | 356-1418 | ||||
Intron_number | 4-8/9 | ||||
Exon_number | 4-10/10 | ||||
Isolation | Mutagen | UV/TMP | |||
Remark | Sequenced by the C. elegans Gene Knockout Consortium | Paper_evidence | WBPaper00041807 | ||
Method | KO_consortium_allele |