WormBase Tree Display for Variation: WBVar00316263
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WBVar00316263 | Evidence | Paper_evidence | WBPaper00036201 | ||
---|---|---|---|---|---|
Name | Public_name | otn19442 | |||
Other_name | OH9482_34812 | ||||
C52E12.11:n.33C>A | |||||
C52E12.2a.2:c.599+706G>T | |||||
C52E12.2a.1:c.599+706G>T | |||||
C52E12.2b.1:c.599+706G>T | |||||
HGVSg | CHROMOSOME_II:g.6997859G>T | ||||
Sequence_details | SMap | S_parent | Sequence | C52E12 | |
Flanking_sequences | CTGAAGCGAATTTTCAATATCCCCGCGTTCATCCATCGTCTCCGCGCTGC | TGACACGACGGTCGGTGGCTGTTCGGCAATCTTTAAATTTTGCATTATTT | |||
Mapping_target | C52E12 | ||||
Type_of_mutation | Substitution | G | T | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00029572 | ||||
Laboratory | OTN | ||||
Analysis | WGS_Hobert | ||||
Status | Live | ||||
Affects | Gene | WBGene00304189 | |||
WBGene00006831 | |||||
Transcript | C52E12.2a.2 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | C52E12.2a.2:c.599+706G>T | ||||
Intron_number | 5/23 | ||||
C52E12.2b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C52E12.2b.1:c.599+706G>T | ||||
Intron_number | 5/24 | ||||
C52E12.2a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C52E12.2a.1:c.599+706G>T | ||||
Intron_number | 5/23 | ||||
Pseudogene | C52E12.11 | VEP_consequence | non_coding_transcript_exon_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | C52E12.11:n.33C>A | ||||
cDNA_position | 33 | ||||
Exon_number | 1/2 | ||||
Genetics | Map | II | |||
Reference | WBPaper00036201 | ||||
Method | WGS_Hobert |