WormBase Tree Display for Variation: WBVar00095025
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WBVar00095025 | Evidence | Paper_evidence | WBPaper00031000 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | ox374 | |||||
Other_name | CE41563:p.Gln2852Ter | ||||||
CE43592:p.Gln2890Ter | |||||||
CE47217:p.Gln2822Ter | |||||||
F25C8.3a.1:c.8554C>T | |||||||
CE47117:p.Gln2831Ter | |||||||
F25C8.3b.1:c.8491C>T | |||||||
F25C8.3c.1:c.8464C>T | |||||||
CE47428:p.Gln2787Ter | |||||||
F25C8.3e.1:c.8359C>T | |||||||
F25C8.3d.1:c.8668C>T | |||||||
HGVSg | CHROMOSOME_V:g.20896927C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | F25C8 | |||
Flanking_sequences | aaagatctgtcacaatgcttgacagtcatg | aaaatgcaatttcacctccgcttgtaaaac | |||||
Mapping_target | F25C8 | ||||||
Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00031000 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | EG | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00006812 | |||||
Transcript | F25C8.3d.1 | VEP_consequence | stop_gained | ||||
VEP_impact | HIGH | ||||||
HGVSc | F25C8.3d.1:c.8668C>T | ||||||
HGVSp | CE43592:p.Gln2890Ter | ||||||
cDNA_position | 8668 | ||||||
CDS_position | 8668 | ||||||
Protein_position | 2890 | ||||||
Exon_number | 33/37 | ||||||
Codon_change | Caa/Taa | ||||||
Amino_acid_change | Q/* | ||||||
F25C8.3b.1 | VEP_consequence | stop_gained | |||||
VEP_impact | HIGH | ||||||
HGVSc | F25C8.3b.1:c.8491C>T | ||||||
HGVSp | CE47117:p.Gln2831Ter | ||||||
cDNA_position | 8744 | ||||||
CDS_position | 8491 | ||||||
Protein_position | 2831 | ||||||
Exon_number | 31/36 | ||||||
Codon_change | Caa/Taa | ||||||
Amino_acid_change | Q/* | ||||||
F25C8.3e.1 | VEP_consequence | stop_gained | |||||
VEP_impact | HIGH | ||||||
HGVSc | F25C8.3e.1:c.8359C>T | ||||||
HGVSp | CE47428:p.Gln2787Ter | ||||||
cDNA_position | 8359 | ||||||
CDS_position | 8359 | ||||||
Protein_position | 2787 | ||||||
Exon_number | 29/34 | ||||||
Codon_change | Caa/Taa | ||||||
Amino_acid_change | Q/* | ||||||
F25C8.3c.1 | VEP_consequence | stop_gained | |||||
VEP_impact | HIGH | ||||||
HGVSc | F25C8.3c.1:c.8464C>T | ||||||
HGVSp | CE47217:p.Gln2822Ter | ||||||
cDNA_position | 8464 | ||||||
CDS_position | 8464 | ||||||
Protein_position | 2822 | ||||||
Exon_number | 31/35 | ||||||
Codon_change | Caa/Taa | ||||||
Amino_acid_change | Q/* | ||||||
F25C8.3a.1 | VEP_consequence | stop_gained | |||||
VEP_impact | HIGH | ||||||
HGVSc | F25C8.3a.1:c.8554C>T | ||||||
HGVSp | CE41563:p.Gln2852Ter | ||||||
cDNA_position | 8554 | ||||||
CDS_position | 8554 | ||||||
Protein_position | 2852 | ||||||
Exon_number | 32/37 | ||||||
Codon_change | Caa/Taa | ||||||
Amino_acid_change | Q/* | ||||||
Genetics | Interpolated_map_position | V | 25.6129 | ||||
Reference | WBPaper00031000 | ||||||
Method | Substitution_allele |