WormBase Tree Display for Variation: WBVar00094760
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WBVar00094760 | Evidence | Paper_evidence | WBPaper00031316 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | os21 | |||||
Other_name | T05G5.9a.1:c.1507-149A>C | ||||||
T05G5.9b.1:c.1501-149A>C | |||||||
HGVSg | CHROMOSOME_III:g.9759013T>G | ||||||
Sequence_details | SMap | S_parent | Sequence | T05G5 | |||
Flanking_sequences | attcggttttgatctctgaatgttcatttt | gttttgttgcgcgcgcgcgcgcgagaaatt | |||||
Mapping_target | T05G5 | ||||||
Type_of_mutation | Substitution | t | g | Paper_evidence | WBPaper00031316 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | HS | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00011503 | |||||
Transcript | T05G5.9b.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | ||||||
HGVSc | T05G5.9b.1:c.1501-149A>C | ||||||
Intron_number | 7/10 | ||||||
T05G5.9a.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | T05G5.9a.1:c.1507-149A>C | ||||||
Intron_number | 7/11 | ||||||
Genetics | Interpolated_map_position | III | 0.990827 | ||||
Reference | WBPaper00031316 | ||||||
Method | Substitution_allele |