WormBase Tree Display for Variation: WBVar01462647
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WBVar01462647 | Evidence | Paper_evidence | WBPaper00040707 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar01462647 | |||
Other_name | cewivar00585159 | ||||
F35E12.6.1:c.703T>G | |||||
F35E12.6.2:c.703T>G | |||||
CE35523:p.Ser235Ala | |||||
HGVSg | CHROMOSOME_V:g.13734956A>C | ||||
Sequence_details | SMap | S_parent | Sequence | F35E12 | |
Flanking_sequences | ATATAAATTCTAATGAGAAATAGTTACCTG | TGCGTCGTTTGCAAGTAACATTGAATTAGA | |||
Mapping_target | F35E12 | ||||
Type_of_mutation | Substitution | a | c | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Natural_variant | |||||
Origin (7) | |||||
Affects | Gene | WBGene00009430 | |||
Transcript | F35E12.6.1 | VEP_consequence | missense_variant | ||
VEP_impact | MODERATE | ||||
HGVSc | F35E12.6.1:c.703T>G | ||||
HGVSp | CE35523:p.Ser235Ala | ||||
cDNA_position | 706 | ||||
CDS_position | 703 | ||||
Protein_position | 235 | ||||
Exon_number | 7/11 | ||||
Codon_change | Tca/Gca | ||||
Amino_acid_change | S/A | ||||
F35E12.6.2 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | F35E12.6.2:c.703T>G | ||||
HGVSp | CE35523:p.Ser235Ala | ||||
cDNA_position | 743 | ||||
CDS_position | 703 | ||||
Protein_position | 235 | ||||
Exon_number | 8/12 | ||||
Codon_change | Tca/Gca | ||||
Amino_acid_change | S/A | ||||
Reference | WBPaper00040707 | ||||
Method | WGS_Andersen |