WormBase Tree Display for Variation: WBVar00115310
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WBVar00115310 | Evidence | Paper_evidence | WBPaper00030778 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00115310 | |||
Other_name | cbs50831 | ||||
HGVSg | chrIII:g.8589352C>T | ||||
Sequence_details | SMap | S_parent | Sequence | cb25.fpc2234 | |
Flanking_sequences | atgaagcatttgatggagcaacttggcattgtggtccagtccatccatca | tacagacacaagtgatgttgtttgtggctgtattgtgaacacaatctcca | |||
Mapping_target | cb25.fpc2234 | ||||
Type_of_mutation | Substitution | G | A | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
RFLP | Reference_strain_digest (27) | ||||
Polymorphic_strain_digest (27) | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis briggsae | |||
Strain | WBStrain00041077 | ||||
Laboratory | CP | ||||
Person | WBPerson3706 | ||||
WBPerson227 | |||||
WBPerson225 | |||||
Status | Live | ||||
Affects | Gene | WBGene00031318 | |||
Transcript | CBG09798a.1 | VEP_consequence | missense_variant | ||
VEP_impact | MODERATE | ||||
HGVSc | CBG09798a.1:c.10220C>T | ||||
HGVSp | CBP47285.1:p.Thr3407Ile | ||||
cDNA_position | 10220 | ||||
CDS_position | 10220 | ||||
Protein_position | 3407 | ||||
Exon_number | 31/34 | ||||
Codon_change | aCt/aTt | ||||
Amino_acid_change | T/I | ||||
CBG09798b.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | CBG09798b.1:c.10277C>T | ||||
HGVSp | CBP41439.1:p.Thr3426Ile | ||||
cDNA_position | 10277 | ||||
CDS_position | 10277 | ||||
Protein_position | 3426 | ||||
Exon_number | 32/35 | ||||
Codon_change | aCt/aTt | ||||
Amino_acid_change | T/I | ||||
CBG09798c.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | CBG09798c.1:c.8453C>T | ||||
HGVSp | CBP38221.1:p.Thr2818Ile | ||||
cDNA_position | 8453 | ||||
CDS_position | 8453 | ||||
Protein_position | 2818 | ||||
Exon_number | 21/24 | ||||
Codon_change | aCt/aTt | ||||
Amino_acid_change | T/I | ||||
Reference | WBPaper00030778 | ||||
Remark | Predicted by: ssaha-SNP v2.0 | ||||
This SNP was observed in 1 sequencing read(s) | |||||
Method | SNP |