WormBase Tree Display for Variation: WBVar01443192
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WBVar01443192 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01443192 | ||||
Other_name | W02B3.4.1:c.1059C>T | |||||
CE34600:p.His353= | ||||||
HGVSg | CHROMOSOME_III:g.681001G>A | |||||
Sequence_details | SMap | S_parent | Sequence | W02B3 | ||
Flanking_sequences | TGAAGAATTCCATGAGTACTTTGATGTCAG | TGATCGAGGTACCATAGTTGGCCATACTCT | ||||
Mapping_target | W02B3 | |||||
Type_of_mutation | Substitution | g | a | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00005835 | From_analysis | WGS_Andersen | |||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | WGS_Andersen | |||||
DB_info | Database | dbSNP_rs | rs | 193330353 | ||
dbSNP_ss | ss | 295506272 | ||||
Status | Live | |||||
Affects | Gene | WBGene00020924 | ||||
Transcript | W02B3.4.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | |||||
HGVSc | W02B3.4.1:c.1059C>T | |||||
HGVSp | CE34600:p.His353= | |||||
cDNA_position | 1148 | |||||
CDS_position | 1059 | |||||
Protein_position | 353 | |||||
Exon_number | 9/10 | |||||
Codon_change | caC/caT | |||||
Amino_acid_change | H | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |