WormBase Tree Display for Variation: WBVar00083093
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WBVar00083093 | Name | Public_name | WBVar00083093 | ||
---|---|---|---|---|---|
Other_name (12) | |||||
HGVSg | CHROMOSOME_X:g.11274060T>C | ||||
Sequence_details | SMap | S_parent | Sequence | C03A3 | |
Flanking_sequences | aacgtcgtattgctcagcttgagga | gaggtgaagcggatcaagcaagaga | |||
Mapping_target | C03A3 | ||||
Type_of_mutation | Substitution | T | C | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00004602 | From_analysis | Million_mutation_project_reanalysis | ||
WGS_Hawaiian_Waterston | |||||
WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | |||
WBStrain00027647 | From_analysis | Million_mutation_project_reanalysis | |||
Laboratory | RW | ||||
Person | WBPerson1562 | ||||
Analysis | WGS_Hawaiian_Waterston | ||||
Million_mutation_project_reanalysis | |||||
Status | Live | ||||
Affects | Gene | WBGene00002050 | |||
Transcript | F38B2.1b.1 | VEP_consequence | synonymous_variant | ||
VEP_impact | LOW | ||||
HGVSc | F38B2.1b.1:c.594T>C | ||||
HGVSp | CE31507:p.Asp198= | ||||
cDNA_position | 700 | ||||
CDS_position | 594 | ||||
Protein_position | 198 | ||||
Exon_number | 7/11 | ||||
Codon_change | gaT/gaC | ||||
Amino_acid_change | D | ||||
F38B2.1d.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | F38B2.1d.1:c.645T>C | ||||
HGVSp | CE24961:p.Asp215= | ||||
cDNA_position | 645 | ||||
CDS_position | 645 | ||||
Protein_position | 215 | ||||
Exon_number | 6/9 | ||||
Codon_change | gaT/gaC | ||||
Amino_acid_change | D | ||||
F38B2.1a.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | F38B2.1a.1:c.594T>C | ||||
HGVSp | CE31506:p.Asp198= | ||||
cDNA_position | 660 | ||||
CDS_position | 594 | ||||
Protein_position | 198 | ||||
Exon_number | 7/11 | ||||
Codon_change | gaT/gaC | ||||
Amino_acid_change | D | ||||
F38B2.1e.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | F38B2.1e.1:c.681T>C | ||||
HGVSp | CE53169:p.Asp227= | ||||
cDNA_position | 681 | ||||
CDS_position | 681 | ||||
Protein_position | 227 | ||||
Exon_number | 6/10 | ||||
Codon_change | gaT/gaC | ||||
Amino_acid_change | D | ||||
F38B2.1c.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | F38B2.1c.1:c.570T>C | ||||
HGVSp | CE05824:p.Asp190= | ||||
cDNA_position | 572 | ||||
CDS_position | 570 | ||||
Protein_position | 190 | ||||
Exon_number | 6/10 | ||||
Codon_change | gaT/gaC | ||||
Amino_acid_change | D | ||||
Remark | [20081124 db] this Variation was previously named hw107453 | ||||
Method | WGS_Hawaiian_Waterston |