WormBase Tree Display for Variation: WBVar00115304
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WBVar00115304 | Evidence | Paper_evidence | WBPaper00030778 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00115304 | |||
Other_name | cbs50825 | ||||
HGVSg | chrIII:g.8589298C>G | ||||
Sequence_details | SMap | S_parent | Sequence | cb25.fpc2234 | |
Flanking_sequences | agacacaagtgatgttgtttgtggctgtattgtgaacacaatctccatga | cattgcataaatcacagaggagagctccacaaactcttcctggctcgtct | |||
Mapping_target | cb25.fpc2234 | ||||
Type_of_mutation | Substitution | G | C | ||
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.10166C>G | ||||
HGVSp | CBP47285.1:p.Ala3389Gly | ||||
cDNA_position | 10166 | ||||
CDS_position | 10166 | ||||
Protein_position | 3389 | ||||
Exon_number | 31/34 | ||||
Codon_change | gCt/gGt | ||||
Amino_acid_change | A/G | ||||
CBG09798b.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | CBG09798b.1:c.10223C>G | ||||
HGVSp | CBP41439.1:p.Ala3408Gly | ||||
cDNA_position | 10223 | ||||
CDS_position | 10223 | ||||
Protein_position | 3408 | ||||
Exon_number | 32/35 | ||||
Codon_change | gCt/gGt | ||||
Amino_acid_change | A/G | ||||
CBG09798c.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | CBG09798c.1:c.8399C>G | ||||
HGVSp | CBP38221.1:p.Ala2800Gly | ||||
cDNA_position | 8399 | ||||
CDS_position | 8399 | ||||
Protein_position | 2800 | ||||
Exon_number | 21/24 | ||||
Codon_change | gCt/gGt | ||||
Amino_acid_change | A/G | ||||
Reference | WBPaper00030778 | ||||
Remark | Predicted by: ssaha-SNP v2.0 | ||||
This SNP was observed in 1 sequencing read(s) | |||||
Method | SNP |