WormBase Tree Display for Variation: WBVar00104544
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WBVar00104544 | Evidence | Paper_evidence | WBPaper00040707 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00104544 | |||
Other_name | pas9403 | ||||
cewivar00091311 | |||||
C52E12.2a.2:c.1932G>T | |||||
CE48050:p.Val644= | |||||
C52E12.2a.1:c.1932G>T | |||||
CE47855:p.Val644= | |||||
C52E12.2b.1:c.1932G>T | |||||
HGVSg | CHROMOSOME_II:g.7003950G>T | ||||
Sequence_details | SMap | S_parent | Sequence | C52E12 | |
Flanking_sequences | gcagcaatagctggttagttcagaaaaatcattttaatcaaaggtttaaaataattgtagaacaaccaattgattggaaatatgctcaacaagaacttctagacaaacaaggaattgatctaaaagcagatatggagaagaaaatgttagaaatggaatctcaatacagaagagaaaaagtagaattggaacaaaaaatgtatcatcagacaagggtaaacctacattcatttgtaaatatttaaaaaaataaatttcttaggaatatgaatcaatgattgaaaatcttcaaaaacaagt | gatttggcacaatcttatatatctggtggtggttctatttgggaaggagaacgaatgttgacgtcatctttacttgaattccgtaagtgctctttttttgaaaggcggcgattgttttcaaagatattacaatttattcatttttgaaaactgcttaacaccagtgaaactttttcatccattattgtttgaaatcacaagattatatttttcaaacagctctaatgtttcgtaagtttggcaatttgccaaactatttagatatatcccaactgacgctatttcgccttttaaaatgtt | |||
Mapping_target | C52E12 | ||||
Type_of_mutation | Substitution | G | T | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain (29) | |||||
Laboratory | QX | ||||
Person | WBPerson6900 | ||||
WBPerson1730 | |||||
Analysis | WGS_Pasadena_Quinlan | ||||
Million_mutation_project_reanalysis | |||||
WGS_Andersen | |||||
History | Acquires_merge | WBVar01438339 | |||
Status | Live | ||||
Affects | Gene | WBGene00006831 | |||
Transcript | C52E12.2a.2 | VEP_consequence | synonymous_variant | ||
VEP_impact | LOW | ||||
HGVSc | C52E12.2a.2:c.1932G>T | ||||
HGVSp | CE48050:p.Val644= | ||||
cDNA_position | 1934 | ||||
CDS_position | 1932 | ||||
Protein_position | 644 | ||||
Exon_number | 11/24 | ||||
Codon_change | gtG/gtT | ||||
Amino_acid_change | V | ||||
C52E12.2b.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | C52E12.2b.1:c.1932G>T | ||||
HGVSp | CE47855:p.Val644= | ||||
cDNA_position | 2132 | ||||
CDS_position | 1932 | ||||
Protein_position | 644 | ||||
Exon_number | 11/25 | ||||
Codon_change | gtG/gtT | ||||
Amino_acid_change | V | ||||
C52E12.2a.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | C52E12.2a.1:c.1932G>T | ||||
HGVSp | CE48050:p.Val644= | ||||
cDNA_position | 2068 | ||||
CDS_position | 1932 | ||||
Protein_position | 644 | ||||
Exon_number | 11/24 | ||||
Codon_change | gtG/gtT | ||||
Amino_acid_change | V | ||||
Reference | WBPaper00040707 | ||||
Method | WGS_Pasadena_Quinlan |