WormBase Tree Display for Variation: WBVar01744375
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WBVar01744375 | Name | Public_name | WBVar01744375 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00443659 | |||||||
T16A9.3.3:c.441C>T | ||||||||
T16A9.3.2:c.441C>T | ||||||||
T16A9.3.1:c.441C>T | ||||||||
CE43662:p.His147= | ||||||||
HGVSg | CHROMOSOME_V:g.14208151C>T | |||||||
Sequence_details | SMap | S_parent | Sequence | T16A9 | ||||
Flanking_sequences | TTATTACCAATTTAATTCCAGATCCCGCCA | AATTTGATGCTAAAAACATCCGACGGCGTC | ||||||
Mapping_target | T16A9 | |||||||
Source_location | 225 | CHROMOSOME_V | 14208136 | 14208136 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | C | T | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022930 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00023139 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027648 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027660 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027662 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00011793 | ||||||
Transcript | T16A9.3.3 | VEP_consequence | synonymous_variant | |||||
VEP_impact | LOW | |||||||
HGVSc | T16A9.3.3:c.441C>T | |||||||
HGVSp | CE43662:p.His147= | |||||||
cDNA_position | 1172 | |||||||
CDS_position | 441 | |||||||
Protein_position | 147 | |||||||
Exon_number | 5/9 | |||||||
Codon_change | caC/caT | |||||||
Amino_acid_change | H | |||||||
T16A9.3.2 | VEP_consequence | synonymous_variant | ||||||
VEP_impact | LOW | |||||||
HGVSc | T16A9.3.2:c.441C>T | |||||||
HGVSp | CE43662:p.His147= | |||||||
cDNA_position | 591 | |||||||
CDS_position | 441 | |||||||
Protein_position | 147 | |||||||
Exon_number | 4/8 | |||||||
Codon_change | caC/caT | |||||||
Amino_acid_change | H | |||||||
T16A9.3.1 | VEP_consequence | synonymous_variant | ||||||
VEP_impact | LOW | |||||||
HGVSc | T16A9.3.1:c.441C>T | |||||||
HGVSp | CE43662:p.His147= | |||||||
cDNA_position | 899 | |||||||
CDS_position | 441 | |||||||
Protein_position | 147 | |||||||
Exon_number | 6/10 | |||||||
Codon_change | caC/caT | |||||||
Amino_acid_change | H | |||||||
Method | WGS_Flibotte |