WormBase Tree Display for Variation: WBVar00091771
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WBVar00091771 | Name | Public_name | ok483 | ||
---|---|---|---|---|---|
Other_name | T21G5.5b.1:c.303+47_983+269del | ||||
T21G5.5c.1:c.429+47_1109+269del | |||||
T21G5.5d.2:c.519+47_1199+269del | |||||
T21G5.5d.1:c.519+47_1199+269del | |||||
T21G5.5b.2:c.303+47_983+269del | |||||
HGVSg | CHROMOSOME_I:g.6879505_6881200del | ||||
Sequence_details | SMap | S_parent | Sequence | T21G5 | |
Flanking_sequences | ccttactccaccttcaagtgtttaggagat | ttgttttgttattaaaaaaaagttttagaa | |||
Mapping_target | T21G5 | ||||
Type_of_mutation | Deletion | ||||
PCR_product | OK483_external | ||||
OK483_internal | |||||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00035620 | ||||
Laboratory | RB | ||||
Person | WBPerson46 | ||||
KO_consortium_allele | |||||
Status | Live | ||||
Affects | Gene | WBGene00006423 | |||
Transcript | T21G5.5d.2 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant | ||
VEP_impact | HIGH | ||||
HGVSc | T21G5.5d.2:c.519+47_1199+269del | ||||
Intron_number | 4-6/8 | ||||
Exon_number | 5-6/9 | ||||
T21G5.5b.1 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | T21G5.5b.1:c.303+47_983+269del | ||||
Intron_number | 5-7/8 | ||||
Exon_number | 6-7/9 | ||||
T21G5.5c.1 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | T21G5.5c.1:c.429+47_1109+269del | ||||
Intron_number | 3-5/6 | ||||
Exon_number | 4-5/7 | ||||
T21G5.5b.2 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | T21G5.5b.2:c.303+47_983+269del | ||||
Intron_number | 3-5/6 | ||||
Exon_number | 4-5/7 | ||||
T21G5.5a.1 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant | |||
VEP_impact | HIGH | ||||
Intron_number | 3-4/4 | ||||
Exon_number | 4-5/5 | ||||
T21G5.5d.1 | VEP_consequence | splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant | |||
VEP_impact | HIGH | ||||
HGVSc | T21G5.5d.1:c.519+47_1199+269del | ||||
Intron_number | 5-7/9 | ||||
Exon_number | 6-7/10 | ||||
Isolation | Mutagen | UV/TMP | |||
Remark | Last updated on 29 Nov 2002 | ||||
Sequenced by the C. elegans Gene Knockout Consortium | Paper_evidence | WBPaper00041807 | |||
Method | KO_consortium_allele |