WormBase Tree Display for Variation: WBVar00140315
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WBVar00140315 | Name | Public_name | WBVar00140315 | ||
---|---|---|---|---|---|
Other_name | cbh44841 | ||||
HGVSg | chrV:g.2273190C>T | ||||
Sequence_details (5) | |||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis briggsae | |||
Strain | WBStrain00041078 | ||||
Laboratory | CP | ||||
Person | WBPerson3706 | ||||
WBPerson227 | |||||
WBPerson225 | |||||
Status | Live | ||||
Affects | Gene | WBGene00042654 | |||
Transcript | CBG24578a.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | CBG24578a.1:c.1121-418G>A | ||||
Intron_number | 7/11 | ||||
CBG24578b.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | CBG24578b.1:c.1209G>A | ||||
HGVSp | CBP40114.1:p.Ala403%3D | ||||
cDNA_position | 1218 | ||||
CDS_position | 1209 | ||||
Protein_position | 403 | ||||
Exon_number | 8/11 | ||||
Codon_change | gcG/gcA | ||||
Amino_acid_change | A | ||||
CBG24578c.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | CBG24578c.1:c.1332G>A | ||||
HGVSp | CBP43939.1:p.Ala444%3D | ||||
cDNA_position | 1332 | ||||
CDS_position | 1332 | ||||
Protein_position | 444 | ||||
Exon_number | 7/10 | ||||
Codon_change | gcG/gcA | ||||
Amino_acid_change | A | ||||
CBG24578d.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | CBG24578d.1:c.1068G>A | ||||
HGVSp | CBP41903.1:p.Ala356%3D | ||||
cDNA_position | 1068 | ||||
CDS_position | 1068 | ||||
Protein_position | 356 | ||||
Exon_number | 7/10 | ||||
Codon_change | gcG/gcA | ||||
Amino_acid_change | A | ||||
CBG24578e.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | CBG24578e.1:c.986-418G>A | ||||
Intron_number | 7/11 | ||||
CBG24578f.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | CBG24578f.1:c.986-418G>A | ||||
Intron_number | 7/10 | ||||
CBG24578g.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | CBG24578g.1:c.1121-418G>A | ||||
Intron_number | 7/10 | ||||
Method | SNP |