WormBase Tree Display for Variation: WBVar00584115
expand all nodes | collapse all nodes | view schema
WBVar00584115 | Evidence | Paper_evidence | WBPaper00038208 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00584115 | |||
Other_name (11) | |||||
HGVSg | CHROMOSOME_V:g.3706945A>T | ||||
Sequence_details | SMap | S_parent | Sequence | T27C4 | |
Flanking_sequences | CCGTGTGAGAATTGCGGGACGCTGGACGCTCTCAACTGGTATCAGTGGGG | GGTGTCGGCGATAAGAAGGTTCTGTGCTCGACGTGTTGGATTCAGTGGAA | |||
Mapping_target | T27C4 | ||||
Type_of_mutation | Substitution | a | t | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00004602 | From_analysis | Million_mutation_project_reanalysis | ||
WGS_Yanai | |||||
Person | WBPerson4037 | ||||
Analysis | WGS_Yanai | ||||
Million_mutation_project_reanalysis | |||||
Status | Live | ||||
Affects | Gene | WBGene00003025 | |||
Transcript | T27C4.4d.1 | VEP_consequence | synonymous_variant | ||
VEP_impact | LOW | ||||
HGVSc | T27C4.4d.1:c.1806A>T | ||||
HGVSp | CE33331:p.Gly602= | ||||
cDNA_position | 1830 | ||||
CDS_position | 1806 | ||||
Protein_position | 602 | ||||
Exon_number | 4/9 | ||||
Codon_change | ggA/ggT | ||||
Amino_acid_change | G | ||||
T27C4.4b.2 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | T27C4.4b.2:c.1806A>T | ||||
HGVSp | CE21212:p.Gly602= | ||||
cDNA_position | 1830 | ||||
CDS_position | 1806 | ||||
Protein_position | 602 | ||||
Exon_number | 4/9 | ||||
Codon_change | ggA/ggT | ||||
Amino_acid_change | G | ||||
T27C4.4a.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | T27C4.4a.1:c.1806A>T | ||||
HGVSp | CE21211:p.Gly602= | ||||
cDNA_position | 1823 | ||||
CDS_position | 1806 | ||||
Protein_position | 602 | ||||
Exon_number | 4/10 | ||||
Codon_change | ggA/ggT | ||||
Amino_acid_change | G | ||||
T27C4.4e.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | T27C4.4e.1:c.1401A>T | ||||
HGVSp | CE51633:p.Gly467= | ||||
cDNA_position | 1401 | ||||
CDS_position | 1401 | ||||
Protein_position | 467 | ||||
Exon_number | 1/5 | ||||
Codon_change | ggA/ggT | ||||
Amino_acid_change | G | ||||
T27C4.4b.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | T27C4.4b.1:c.1806A>T | ||||
HGVSp | CE21212:p.Gly602= | ||||
cDNA_position | 1823 | ||||
CDS_position | 1806 | ||||
Protein_position | 602 | ||||
Exon_number | 4/9 | ||||
Codon_change | ggA/ggT | ||||
Amino_acid_change | G | ||||
Reference | WBPaper00038208 | ||||
Method | WGS_Yanai |