WormBase Tree Display for Variation: WBVar00090149
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WBVar00090149 | Evidence | Paper_evidence | WBPaper00002518 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | n1378 | |||||
Other_name | CE17673:p.Gln569Ter | ||||||
F15C11.1.1:c.1705C>T | |||||||
HGVSg | CHROMOSOME_I:g.7047462C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | F15C11 | |||
Flanking_sequences | ccaaaaaacgaaaatccactgcttgcaatg | aaaaaatgtgggcggagacagagccaccac | |||||
Mapping_target | F15C11 | ||||||
Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00002518 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain (8) | |||||||
Laboratory | MT | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00004773 | |||||
Transcript | F15C11.1.1 | VEP_consequence | stop_gained | ||||
VEP_impact | HIGH | ||||||
HGVSc | F15C11.1.1:c.1705C>T | ||||||
HGVSp | CE17673:p.Gln569Ter | ||||||
cDNA_position | 1713 | ||||||
CDS_position | 1705 | ||||||
Protein_position | 569 | ||||||
Exon_number | 9/12 | ||||||
Codon_change | Caa/Taa | ||||||
Amino_acid_change | Q/* | ||||||
Genetics | Interpolated_map_position | I | 1.66236 | ||||
Mapping_data | In_multi_point | 1446 | |||||
1447 | |||||||
2089 | |||||||
Description (2) | |||||||
Reference | WBPaper00006052 | ||||||
WBPaper00022358 | |||||||
WBPaper00014018 | |||||||
WBPaper00011119 | |||||||
WBPaper00001105 | |||||||
WBPaper00014234 | |||||||
WBPaper00017445 | |||||||
WBPaper00002518 | |||||||
WBPaper00051369 | |||||||
Method | Substitution_allele |