WormBase Tree Display for Variation: WBVar01446379
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WBVar01446379 | Evidence | Paper_evidence | WBPaper00040707 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar01446379 | |||
Other_name | F57B9.5.1:c.*37A>C | ||||
HGVSg | CHROMOSOME_III:g.6935690A>C | ||||
Sequence_details | SMap | S_parent | Sequence | F57B9 | |
Flanking_sequences | CACAAACAGAAAGAGACGCAGAAGAGAAAT | TTTCCCGCTTTCACTCTATTCTGCACGTAG | |||
Mapping_target | F57B9 | ||||
Type_of_mutation | Substitution | a | c | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Natural_variant | |||||
Origin (7) | |||||
Affects | Gene | WBGene00000276 | |||
WBGene00305460 | |||||
Transcript | F57B9.5.1 | VEP_consequence | 3_prime_UTR_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | F57B9.5.1:c.*37A>C | ||||
cDNA_position | 1391 | ||||
Exon_number | 12/12 | ||||
F57B9.13 | |||||
Reference | WBPaper00040707 | ||||
Method | WGS_Andersen |