WormBase Tree Display for Variation: WBVar01686418
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WBVar01686418 | Name | Public_name | WBVar01686418 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00377863 | |||||||
CE44055:p.Gly1316= | ||||||||
F53A3.4d.1:c.-919G>A | ||||||||
CE44091:p.Gly1316= | ||||||||
F53A3.4c.1:c.3948G>A | ||||||||
CE44019:p.Gly1316= | ||||||||
F53A3.4b.1:c.3948G>A | ||||||||
F53A3.4d.2:c.-919G>A | ||||||||
F53A3.4d.3:c.-868G>A | ||||||||
F53A3.4a.1:c.3948G>A | ||||||||
HGVSg | CHROMOSOME_III:g.1930849G>A | |||||||
Sequence_details | SMap | S_parent | Sequence | F53A3 | ||||
Flanking_sequences | AACCACCAGCGGAGGAGCCGGCCTAATCGG | ATCTCAGCAGCAACTCAGGCTCAACTTCAA | ||||||
Mapping_target | F53A3 | |||||||
Source_location | 225 | CHROMOSOME_III | 1930840 | 1930840 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | A | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00006640 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00008273 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00305433 | ||||||
WBGene00004128 | ||||||||
Transcript | F53A3.4d.2 | VEP_consequence | 5_prime_UTR_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53A3.4d.2:c.-919G>A | |||||||
cDNA_position | 759 | |||||||
Exon_number | 3/11 | |||||||
F53A3.4d.1 | VEP_consequence | 5_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53A3.4d.1:c.-919G>A | |||||||
cDNA_position | 1083 | |||||||
Exon_number | 4/12 | |||||||
F53A3.4c.1 | VEP_consequence | synonymous_variant | ||||||
VEP_impact | LOW | |||||||
HGVSc | F53A3.4c.1:c.3948G>A | |||||||
HGVSp | CE44091:p.Gly1316= | |||||||
cDNA_position | 3948 | |||||||
CDS_position | 3948 | |||||||
Protein_position | 1316 | |||||||
Exon_number | 17/17 | |||||||
Codon_change | ggG/ggA | |||||||
Amino_acid_change | G | |||||||
F53A3.4b.1 | VEP_consequence | synonymous_variant | ||||||
VEP_impact | LOW | |||||||
HGVSc | F53A3.4b.1:c.3948G>A | |||||||
HGVSp | CE44055:p.Gly1316= | |||||||
cDNA_position | 3948 | |||||||
CDS_position | 3948 | |||||||
Protein_position | 1316 | |||||||
Exon_number | 17/24 | |||||||
Codon_change | ggG/ggA | |||||||
Amino_acid_change | G | |||||||
F53A3.12 | ||||||||
F53A3.4a.1 | VEP_consequence | synonymous_variant | ||||||
VEP_impact | LOW | |||||||
HGVSc | F53A3.4a.1:c.3948G>A | |||||||
HGVSp | CE44019:p.Gly1316= | |||||||
cDNA_position | 3957 | |||||||
CDS_position | 3948 | |||||||
Protein_position | 1316 | |||||||
Exon_number | 18/24 | |||||||
Codon_change | ggG/ggA | |||||||
Amino_acid_change | G | |||||||
F53A3.4d.3 | VEP_consequence | 5_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53A3.4d.3:c.-868G>A | |||||||
cDNA_position | 755 | |||||||
Exon_number | 3/11 | |||||||
Method | WGS_Flibotte |