WormBase Tree Display for Variation: WBVar00296575
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WBVar00296575 | Evidence | Paper_evidence | WBPaper00036466 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | bp238 | |||||
Other_name | F59G1.10:n.66C>T | ||||||
F59G1.4a.1:c.947-151G>A | |||||||
HGVSg | CHROMOSOME_II:g.5902290G>A | ||||||
Sequence_details | SMap | S_parent | Sequence | F59G1 | |||
Flanking_sequences | ccggcctgttccctgagacctcaagtgtga | tgtactattgatgcttcacacctgggctct | |||||
Mapping_target | F59G1 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00036466 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | HZ | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00002993 | |||||
WBGene00197123 | |||||||
WBGene00019128 | |||||||
Transcript | F59G1.6 | ||||||
F59G1.10 | VEP_consequence | non_coding_transcript_exon_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F59G1.10:n.66C>T | ||||||
cDNA_position | 66 | ||||||
Exon_number | 1/1 | ||||||
F59G1.4a.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F59G1.4a.1:c.947-151G>A | ||||||
Intron_number | 10/14 | ||||||
Genetics | Interpolated_map_position | II | -0.855222 | ||||
Reference | WBPaper00036466 | ||||||
Method | Substitution_allele |