WormBase Tree Display for Variation: WBVar00241633
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WBVar00241633 | Evidence | Paper_evidence | WBPaper00005585 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | rt58 | |||||
Other_name | F52C9.8a.4:c.1825C>T | ||||||
F52C9.8g.1:c.286-1653C>T | |||||||
F52C9.8a.2:c.1825C>T | |||||||
F52C9.8b.1:c.1825C>T | |||||||
F52C9.8a.1:c.1825C>T | |||||||
CE30998:p.Gln609Ter | |||||||
F52C9.8a.3:c.1825C>T | |||||||
F52C9.8c.1:c.286-1653C>T | |||||||
CE30802:p.Gln609Ter | |||||||
HGVSg | CHROMOSOME_III:g.5314060C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | F52C9 | |||
Flanking_sequences | gttaagccaagagtggctccagtgccgccg | aggttccagtgactccaacgaagccagtaa | |||||
Mapping_target | F52C9 | ||||||
Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00005585 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | HA | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00004095 | |||||
Transcript | F52C9.8a.3 | VEP_consequence | stop_gained | ||||
VEP_impact | HIGH | ||||||
HGVSc | F52C9.8a.3:c.1825C>T | ||||||
HGVSp | CE30802:p.Gln609Ter | ||||||
cDNA_position | 1841 | ||||||
CDS_position | 1825 | ||||||
Protein_position | 609 | ||||||
Exon_number | 7/13 | ||||||
Codon_change | Cag/Tag | ||||||
Amino_acid_change | Q/* | ||||||
F52C9.8a.2 | VEP_consequence | stop_gained | |||||
VEP_impact | HIGH | ||||||
HGVSc | F52C9.8a.2:c.1825C>T | ||||||
HGVSp | CE30802:p.Gln609Ter | ||||||
cDNA_position | 1841 | ||||||
CDS_position | 1825 | ||||||
Protein_position | 609 | ||||||
Exon_number | 7/14 | ||||||
Codon_change | Cag/Tag | ||||||
Amino_acid_change | Q/* | ||||||
F52C9.8a.4 | VEP_consequence | stop_gained | |||||
VEP_impact | HIGH | ||||||
HGVSc | F52C9.8a.4:c.1825C>T | ||||||
HGVSp | CE30802:p.Gln609Ter | ||||||
cDNA_position | 1841 | ||||||
CDS_position | 1825 | ||||||
Protein_position | 609 | ||||||
Exon_number | 7/12 | ||||||
Codon_change | Cag/Tag | ||||||
Amino_acid_change | Q/* | ||||||
F52C9.8c.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F52C9.8c.1:c.286-1653C>T | ||||||
Intron_number | 5/11 | ||||||
F52C9.8g.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F52C9.8g.1:c.286-1653C>T | ||||||
Intron_number | 5/11 | ||||||
F52C9.8a.1 | VEP_consequence | stop_gained | |||||
VEP_impact | HIGH | ||||||
HGVSc | F52C9.8a.1:c.1825C>T | ||||||
HGVSp | CE30802:p.Gln609Ter | ||||||
cDNA_position | 1839 | ||||||
CDS_position | 1825 | ||||||
Protein_position | 609 | ||||||
Exon_number | 7/14 | ||||||
Codon_change | Cag/Tag | ||||||
Amino_acid_change | Q/* | ||||||
F52C9.8b.1 | VEP_consequence | stop_gained | |||||
VEP_impact | HIGH | ||||||
HGVSc | F52C9.8b.1:c.1825C>T | ||||||
HGVSp | CE30998:p.Gln609Ter | ||||||
cDNA_position | 1845 | ||||||
CDS_position | 1825 | ||||||
Protein_position | 609 | ||||||
Exon_number | 7/15 | ||||||
Codon_change | Cag/Tag | ||||||
Amino_acid_change | Q/* | ||||||
Genetics | Interpolated_map_position | III | -1.83165 | ||||
Reference | WBPaper00005585 | ||||||
Method | Substitution_allele |