WormBase Tree Display for Variation: WBVar01870914
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WBVar01870914 | Name | Public_name | WBVar01870914 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00585091 | |||||||
CE38511:p.Phe122= | ||||||||
F35E12.7d.1:c.366T>C | ||||||||
F35E12.7c.1:c.366T>C | ||||||||
CE38513:p.Phe122= | ||||||||
F35E12.7a.1:c.366T>C | ||||||||
CE09922:p.Phe122= | ||||||||
F35E12.7b.1:c.366T>C | ||||||||
CE38512:p.Phe122= | ||||||||
HGVSg | CHROMOSOME_V:g.13730175A>G | |||||||
Sequence_details | SMap | S_parent | Sequence | F35E12 | ||||
Flanking_sequences | CTTACTGTCAATGTATGTGTAAGTTGCGAA | AATGTCAAATTTCCAGTTTTAGAGATAACT | ||||||
Mapping_target | F35E12 | |||||||
Source_location | 225 | CHROMOSOME_V | 13730162 | 13730162 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | G | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00023072 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00009431 | ||||||
Transcript | F35E12.7c.1 | VEP_consequence | synonymous_variant | |||||
VEP_impact | LOW | |||||||
HGVSc | F35E12.7c.1:c.366T>C | |||||||
HGVSp | CE38512:p.Phe122= | |||||||
cDNA_position | 377 | |||||||
CDS_position | 366 | |||||||
Protein_position | 122 | |||||||
Exon_number | 5/14 | |||||||
Codon_change | ttT/ttC | |||||||
Amino_acid_change | F | |||||||
F35E12.7b.1 | VEP_consequence | synonymous_variant | ||||||
VEP_impact | LOW | |||||||
HGVSc | F35E12.7b.1:c.366T>C | |||||||
HGVSp | CE38511:p.Phe122= | |||||||
cDNA_position | 375 | |||||||
CDS_position | 366 | |||||||
Protein_position | 122 | |||||||
Exon_number | 5/13 | |||||||
Codon_change | ttT/ttC | |||||||
Amino_acid_change | F | |||||||
F35E12.7a.1 | VEP_consequence | synonymous_variant | ||||||
VEP_impact | LOW | |||||||
HGVSc | F35E12.7a.1:c.366T>C | |||||||
HGVSp | CE09922:p.Phe122= | |||||||
cDNA_position | 369 | |||||||
CDS_position | 366 | |||||||
Protein_position | 122 | |||||||
Exon_number | 5/14 | |||||||
Codon_change | ttT/ttC | |||||||
Amino_acid_change | F | |||||||
F35E12.7d.1 | VEP_consequence | synonymous_variant | ||||||
VEP_impact | LOW | |||||||
HGVSc | F35E12.7d.1:c.366T>C | |||||||
HGVSp | CE38513:p.Phe122= | |||||||
cDNA_position | 377 | |||||||
CDS_position | 366 | |||||||
Protein_position | 122 | |||||||
Exon_number | 5/14 | |||||||
Codon_change | ttT/ttC | |||||||
Amino_acid_change | F | |||||||
Method | WGS_Flibotte |