WormBase Tree Display for Variation: WBVar01431991
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WBVar01431991 | Evidence | Paper_evidence | WBPaper00040707 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar01431991 | |||
Other_name | CE30258:p.Thr1454= | ||||
C48B6.6b.1:c.4368C>T | |||||
C48B6.6a.1:c.4362C>T | |||||
CE53740:p.Thr1456= | |||||
HGVSg | CHROMOSOME_I:g.6905887G>A | ||||
Sequence_details | SMap | S_parent | Sequence | C48B6 | |
Flanking_sequences | AAGTTCTAGAATTCTCAATGTCGCCAAAGT | GTCTCCTCTTTTTTCTAAAAAAATTATCAA | |||
Mapping_target | C48B6 | ||||
Type_of_mutation | Substitution | g | a | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00031279 | From_analysis | WGS_Andersen | ||
WBStrain00031284 | From_analysis | WGS_Andersen | |||
Laboratory | QX | ||||
Person | WBPerson1730 | ||||
Analysis | WGS_Andersen | ||||
DB_info | Database (2) | ||||
Status | Live | ||||
Affects | Gene | WBGene00004879 | |||
Transcript | C48B6.6b.1 | VEP_consequence | synonymous_variant | ||
VEP_impact | LOW | ||||
HGVSc | C48B6.6b.1:c.4368C>T | ||||
HGVSp | CE53740:p.Thr1456= | ||||
cDNA_position | 4368 | ||||
CDS_position | 4368 | ||||
Protein_position | 1456 | ||||
Exon_number | 27/42 | ||||
Codon_change | acC/acT | ||||
Amino_acid_change | T | ||||
C48B6.6a.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | C48B6.6a.1:c.4362C>T | ||||
HGVSp | CE30258:p.Thr1454= | ||||
cDNA_position | 4390 | ||||
CDS_position | 4362 | ||||
Protein_position | 1454 | ||||
Exon_number | 28/44 | ||||
Codon_change | acC/acT | ||||
Amino_acid_change | T | ||||
Reference | WBPaper00040707 | ||||
Method | WGS_Andersen |