WormBase Tree Display for Variation: WBVar00144903
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WBVar00144903 | Evidence | Paper_evidence | WBPaper00006135 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | e2661 | |||||
Other_name | CE28297:p.Ala236Thr | ||||||
F34D6.3.1:c.706G>A | |||||||
HGVSg | CHROMOSOME_II:g.2685257C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | F34D6 | |||
Flanking_sequences | ttcattctcttcgggctcacggtcatttct | cggcgatgaacctcctagtgctccggtttt | |||||
Mapping_target | F34D6 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00006135 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | CB | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00006318 | |||||
Transcript | F34D6.3.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | ||||||
SIFT | 0 | deleterious | |||||
PolyPhen | 1 | probably_damaging | |||||
HGVSc | F34D6.3.1:c.706G>A | ||||||
HGVSp | CE28297:p.Ala236Thr | ||||||
cDNA_position | 756 | ||||||
CDS_position | 706 | ||||||
Protein_position | 236 | ||||||
Exon_number | 7/10 | ||||||
Codon_change | Gcg/Acg | ||||||
Amino_acid_change | A/T | ||||||
Isolation | Mutagen | EMS | Paper_evidence | WBPaper00006135 | |||
Genetics | Interpolated_map_position | II | -12.1453 | ||||
Reference | WBPaper00006135 | ||||||
Method | Substitution_allele |