WormBase Tree Display for Variation: WBVar01262886
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WBVar01262886 | Evidence | Paper_evidence | WBPaper00037807 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | WBVar01262886 | |||||
Other_name (17) | |||||||
HGVSg | CHROMOSOME_III:g.4249643G>A | ||||||
Sequence_details | SMap | S_parent | Sequence | Y44F5A | |||
Flanking_sequences | GGATTCTCAGAAAGAACAAGTGAAATGAACATTCCACCAGCCTGATGAAT | TAATTCATAGATATTGTAACATCATCCAAATCTCCATCATCTCCTTCCAA | |||||
Mapping_target | Y44F5A | ||||||
Type_of_mutation | Substitution | g | A | Paper_evidence | WBPaper00037807 | ||
SeqStatus | Sequenced | ||||||
Variation_type | SNP | ||||||
Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain | WBStrain00006642 | From_analysis | WGS_De_Bono | ||||
WBStrain00006643 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00006645 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00023665 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | AX | ||||||
Analysis | WGS_De_Bono | ||||||
Million_mutation_project_reanalysis | |||||||
DB_info | Database | dbSNP_ss | ss | 539098541 | |||
Status | Live | ||||||
Affects | Gene | WBGene00011604 | |||||
Transcript | T08A11.1e.1 | VEP_consequence | synonymous_variant | ||||
VEP_impact | LOW | ||||||
HGVSc | T08A11.1e.1:c.4884C>T | ||||||
HGVSp | CE54607:p.Tyr1628= | ||||||
cDNA_position | 4884 | ||||||
CDS_position | 4884 | ||||||
Protein_position | 1628 | ||||||
Exon_number | 16/18 | ||||||
Codon_change | taC/taT | ||||||
Amino_acid_change | Y | ||||||
T08A11.1g.1 | VEP_consequence | synonymous_variant | |||||
VEP_impact | LOW | ||||||
HGVSc | T08A11.1g.1:c.4890C>T | ||||||
HGVSp | CE54616:p.Tyr1630= | ||||||
cDNA_position | 4986 | ||||||
CDS_position | 4890 | ||||||
Protein_position | 1630 | ||||||
Exon_number | 17/19 | ||||||
Codon_change | taC/taT | ||||||
Amino_acid_change | Y | ||||||
T08A11.1h.1 | VEP_consequence | synonymous_variant | |||||
VEP_impact | LOW | ||||||
HGVSc | T08A11.1h.1:c.4896C>T | ||||||
HGVSp | CE54610:p.Tyr1632= | ||||||
cDNA_position | 4992 | ||||||
CDS_position | 4896 | ||||||
Protein_position | 1632 | ||||||
Exon_number | 17/19 | ||||||
Codon_change | taC/taT | ||||||
Amino_acid_change | Y | ||||||
T08A11.1d.1 | VEP_consequence | synonymous_variant | |||||
VEP_impact | LOW | ||||||
HGVSc | T08A11.1d.1:c.4890C>T | ||||||
HGVSp | CE54612:p.Tyr1630= | ||||||
cDNA_position | 4986 | ||||||
CDS_position | 4890 | ||||||
Protein_position | 1630 | ||||||
Exon_number | 17/19 | ||||||
Codon_change | taC/taT | ||||||
Amino_acid_change | Y | ||||||
T08A11.1f.1 | VEP_consequence | synonymous_variant | |||||
VEP_impact | LOW | ||||||
HGVSc | T08A11.1f.1:c.4890C>T | ||||||
HGVSp | CE54622:p.Tyr1630= | ||||||
cDNA_position | 4890 | ||||||
CDS_position | 4890 | ||||||
Protein_position | 1630 | ||||||
Exon_number | 16/18 | ||||||
Codon_change | taC/taT | ||||||
Amino_acid_change | Y | ||||||
T08A11.1c.1 | VEP_consequence | synonymous_variant | |||||
VEP_impact | LOW | ||||||
HGVSc | T08A11.1c.1:c.4884C>T | ||||||
HGVSp | CE54609:p.Tyr1628= | ||||||
cDNA_position | 4884 | ||||||
CDS_position | 4884 | ||||||
Protein_position | 1628 | ||||||
Exon_number | 16/18 | ||||||
Codon_change | taC/taT | ||||||
Amino_acid_change | Y | ||||||
T08A11.1b.1 | VEP_consequence | synonymous_variant | |||||
VEP_impact | LOW | ||||||
HGVSc | T08A11.1b.1:c.4884C>T | ||||||
HGVSp | CE54613:p.Tyr1628= | ||||||
cDNA_position | 4980 | ||||||
CDS_position | 4884 | ||||||
Protein_position | 1628 | ||||||
Exon_number | 17/19 | ||||||
Codon_change | taC/taT | ||||||
Amino_acid_change | Y | ||||||
T08A11.1a.1 | VEP_consequence | synonymous_variant | |||||
VEP_impact | LOW | ||||||
HGVSc | T08A11.1a.1:c.4878C>T | ||||||
HGVSp | CE54207:p.Tyr1626= | ||||||
cDNA_position | 4978 | ||||||
CDS_position | 4878 | ||||||
Protein_position | 1626 | ||||||
Exon_number | 17/19 | ||||||
Codon_change | taC/taT | ||||||
Amino_acid_change | Y | ||||||
Reference | WBPaper00037807 | ||||||
Method | WGS_De_Bono |