WormBase Tree Display for Variation: WBVar00000646
expand all nodes | collapse all nodes | view schema
WBVar00000646 | Evidence | Paper_evidence | WBPaper00001872 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | bz3 | |||||
Other_name | T01C8.7.1:c.2164_2166delinsGCA | ||||||
CE39109:p.Trp722Ala | |||||||
HGVSg | CHROMOSOME_X:g.16803533_16803535delinsTGC | ||||||
Sequence_details | SMap | S_parent | Sequence | T01C8 | |||
Flanking_sequences | ctagccgattttggtggacaactcggtctt | tgcggaatatccttccttacctgttgcgaa | |||||
Mapping_target | T01C8 | ||||||
Type_of_mutation | Substitution | tgg | gca | Paper_evidence | WBPaper00001872 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | ZB | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00003168 | |||||
Transcript | T01C8.7.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | ||||||
HGVSc | T01C8.7.1:c.2164_2166delinsGCA | ||||||
HGVSp | CE39109:p.Trp722Ala | ||||||
cDNA_position | 2165-2167 | ||||||
CDS_position | 2164-2166 | ||||||
Protein_position | 722 | ||||||
Exon_number | 16/17 | ||||||
Codon_change | TGG/GCA | ||||||
Amino_acid_change | W/A | ||||||
Genetics | Interpolated_map_position | X | 24.0624 | ||||
Reference | WBPaper00001872 | ||||||
Method | Substitution_allele |