WormBase Tree Display for Variation: WBVar01639968
expand all nodes | collapse all nodes | view schema
WBVar01639968 | Name | Public_name | WBVar01639968 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00321982 | |||||||
CE39613:p.Ala98Ser | ||||||||
R119.6.1:c.292G>T | ||||||||
HGVSg | CHROMOSOME_I:g.383255G>T | |||||||
Sequence_details | SMap | S_parent | Sequence | R119 | ||||
Flanking_sequences | CCACAAAACTCTGCAGCGGCGGCCGCCGCT | CTTCAGATGACAAAAACGTGACAAAATGCG | ||||||
Mapping_target | R119 | |||||||
Source_location | 225 | CHROMOSOME_I | 383258 | 383258 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | T | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain (11) | ||||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006385 | ||||||
Transcript | R119.6.1 | VEP_consequence | missense_variant | |||||
VEP_impact | MODERATE | |||||||
HGVSc | R119.6.1:c.292G>T | |||||||
HGVSp | CE39613:p.Ala98Ser | |||||||
cDNA_position | 299 | |||||||
CDS_position | 292 | |||||||
Protein_position | 98 | |||||||
Exon_number | 4/10 | |||||||
Codon_change | Gct/Tct | |||||||
Amino_acid_change | A/S | |||||||
Method | WGS_Flibotte |