WormBase Tree Display for Variation: WBVar00249026
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WBVar00249026 | Name | Public_name | sy655 | ||||
---|---|---|---|---|---|---|---|
Other_name | F47A4.2.1:c.6424C>T | ||||||
CE16058:p.Gln2142Ter | |||||||
HGVSg | CHROMOSOME_X:g.9814946G>A | ||||||
Sequence_details | SMap | S_parent | Sequence | F47A4 | |||
Flanking_sequences | gttaaaggcggatggaagttcagaatgttc | aaacaactcggttggataaagttgcaaaga | |||||
Mapping_target | F47A4 | ||||||
Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00005632 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | PS | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00001081 | |||||
Transcript | F47A4.2.1 | VEP_consequence | stop_gained | ||||
VEP_impact | HIGH | ||||||
HGVSc | F47A4.2.1:c.6424C>T | ||||||
HGVSp | CE16058:p.Gln2142Ter | ||||||
cDNA_position | 6527 | ||||||
CDS_position | 6424 | ||||||
Protein_position | 2142 | ||||||
Exon_number | 14/21 | ||||||
Codon_change | Caa/Taa | ||||||
Amino_acid_change | Q/* | ||||||
Genetics | Interpolated_map_position | X | 1.69661 | ||||
Method | Substitution_allele |