WormBase Tree Display for Variation: WBVar01466229
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WBVar01466229 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01466229 | ||||
Other_name | Y116F11B.3.2:c.2465G>C | |||||
CE26048:p.Gly822Ala | ||||||
Y116F11B.3.1:c.2465G>C | ||||||
HGVSg | CHROMOSOME_V:g.19824474C>G | |||||
Sequence_details | SMap | S_parent | Sequence | Y116F11B | ||
Flanking_sequences | TTATTACCCATCCCGGTATAAGTGCCTCCT | CGTTGTTAAATGACGTCATATAGGCATTAA | ||||
Mapping_target | Y116F11B | |||||
Type_of_mutation | Substitution | c | g | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00005299 | From_analysis | WGS_Andersen | |||
WBStrain00005300 | From_analysis | WGS_Andersen | ||||
WBStrain00005301 | From_analysis | WGS_Andersen | ||||
WBStrain00005307 | From_analysis | WGS_Andersen | ||||
WBStrain00005311 | From_analysis | WGS_Andersen | ||||
WBStrain00022886 | From_analysis | WGS_Andersen | ||||
Million_mutation_project_reanalysis | ||||||
WBStrain00022888 | From_analysis | WGS_Andersen | ||||
WBStrain00022889 | From_analysis | WGS_Andersen | ||||
WBStrain00022894 | From_analysis | WGS_Andersen | ||||
WBStrain00022898 | From_analysis | WGS_Andersen | ||||
WBStrain00023065 | From_analysis | WGS_Andersen | ||||
WBStrain00023072 | From_analysis | WGS_Andersen | ||||
Million_mutation_project_reanalysis | ||||||
WBStrain00023085 | From_analysis | WGS_Andersen | ||||
WBStrain00023139 | From_analysis | WGS_Andersen | ||||
Million_mutation_project_reanalysis | ||||||
WBStrain00023208 | From_analysis | WGS_Andersen | ||||
WBStrain00023279 | From_analysis | WGS_Andersen | ||||
WBStrain00027648 | From_analysis | WGS_Andersen | ||||
Million_mutation_project_reanalysis | ||||||
WBStrain00027660 | From_analysis | WGS_Andersen | ||||
Million_mutation_project_reanalysis | ||||||
WBStrain00027661 | From_analysis | WGS_Andersen | ||||
WBStrain00027662 | From_analysis | WGS_Andersen | ||||
Million_mutation_project_reanalysis | ||||||
WBStrain00027669 | From_analysis | WGS_Andersen | ||||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | WGS_Andersen | |||||
DB_info | Database | dbSNP_rs | rs | 193351841 | ||
dbSNP_ss | ss | 295527760 | ||||
Status | Live | |||||
Affects | Gene | WBGene00003959 | ||||
Transcript | Y116F11B.3.2 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | |||||
SIFT | 0.01 | deleterious | ||||
PolyPhen | 0.244 | benign | ||||
HGVSc | Y116F11B.3.2:c.2465G>C | |||||
HGVSp | CE26048:p.Gly822Ala | |||||
cDNA_position | 2509 | |||||
CDS_position | 2465 | |||||
Protein_position | 822 | |||||
Exon_number | 7/9 | |||||
Codon_change | gGa/gCa | |||||
Amino_acid_change | G/A | |||||
Y116F11B.3.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | |||||
SIFT | 0.01 | deleterious | ||||
PolyPhen | 0.244 | benign | ||||
HGVSc | Y116F11B.3.1:c.2465G>C | |||||
HGVSp | CE26048:p.Gly822Ala | |||||
cDNA_position | 2474 | |||||
CDS_position | 2465 | |||||
Protein_position | 822 | |||||
Exon_number | 6/8 | |||||
Codon_change | gGa/gCa | |||||
Amino_acid_change | G/A | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |