WormBase Tree Display for Variation: WBVar00102798
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WBVar00102798 | Name | Public_name | WBVar00102798 | ||
---|---|---|---|---|---|
Other_name | pas7657 | ||||
cewivar00088366 | |||||
CE25336:p.Pro39= | |||||
Y49F6B.2.1:c.117T>A | |||||
HGVSg | CHROMOSOME_II:g.3503178T>A | ||||
Sequence_details | SMap | S_parent | Sequence | Y49F6B | |
Flanking_sequences | ttatttcgaaggttttcaccgggttttcgtcggttttcgctctttttcgccagttttttcgaataaaaattgaaattgaatgattttcagctcaaaatgtctgcgctctacttcaaaaagctacgaaaacagcagaatcccgacgtttcaagcagcgaagattcggattccgacgaggaaattccaaaaaagaagcaaaagcaacaagtaatcacaaaaaacggcgatttttgcaaatttttagcgaaaaaaaccgaaaatttcccagaaaagcaccaaaaaaatcgattttcagaagcc | gtcgccgaggaattcgatgatttcgtcgttgacagagccgtacgtgaagaagcgccaaaagaaggagcttttgaggcagttgacctgctcggaacatcctatttggagccatatgagatggataaggacttgcaggagcttctggaaaagtcagttgtcgggccgaagtttgaaggcgatcatcagcctcaaaataggcttttaggccggaatgcggccgccaggctgaagaaagtgcgttgaaatcgatgaaaattcgattaaaatcgctcaaaatccaataaaaatcgctatttttcc | |||
Mapping_target | Y49F6B | ||||
Type_of_mutation | Substitution | T | A | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00000034 | From_analysis | Million_mutation_project_reanalysis | ||
WBStrain00004599 | From_analysis | Million_mutation_project_reanalysis | |||
WBStrain00004604 | From_analysis | WGS_Pasadena_Quinlan | |||
WBStrain00006637 | From_analysis | Million_mutation_project_reanalysis | |||
WBStrain00008273 | From_analysis | Million_mutation_project_reanalysis | |||
WBStrain00022868 | From_analysis | Million_mutation_project_reanalysis | |||
WBStrain00023665 | From_analysis | Million_mutation_project_reanalysis | |||
WBStrain00031113 | From_analysis | Million_mutation_project_reanalysis | |||
Person | WBPerson6900 | ||||
Analysis | WGS_Pasadena_Quinlan | ||||
Million_mutation_project_reanalysis | |||||
Status | Live | ||||
Affects | Gene | WBGene00021715 | |||
Transcript | Y49F6B.2.1 | VEP_consequence | synonymous_variant | ||
VEP_impact | LOW | ||||
HGVSc | Y49F6B.2.1:c.117T>A | ||||
HGVSp | CE25336:p.Pro39= | ||||
cDNA_position | 123 | ||||
CDS_position | 117 | ||||
Protein_position | 39 | ||||
Exon_number | 3/7 | ||||
Codon_change | ccT/ccA | ||||
Amino_acid_change | P | ||||
Method | WGS_Pasadena_Quinlan |