WormBase Tree Display for Variation: WBVar00192015
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WBVar00192015 | Name | Public_name | WBVar00192015 | ||
---|---|---|---|---|---|
Other_name (12) | |||||
HGVSg | CHROMOSOME_IV:g.11341455T>A | ||||
Sequence_details | SMap | S_parent | Sequence | F54E12 | |
Flanking_sequences | gaaaatgatacaattagacagcatt | gatttccagaatccgactgtcgaat | |||
Mapping_target | F54E12 | ||||
Type_of_mutation | Substitution | T | A | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00004602 | From_analysis | Million_mutation_project_reanalysis | ||
WGS_Hawaiian_Waterston | |||||
Laboratory | RW | ||||
Person | WBPerson1562 | ||||
Analysis | WGS_Hawaiian_Waterston | ||||
Million_mutation_project_reanalysis | |||||
Status | Live | ||||
Affects | Gene | WBGene00001931 | |||
WBGene00002223 | |||||
Transcript | T01G1.1d.1 | VEP_consequence | synonymous_variant | ||
VEP_impact | LOW | ||||
HGVSc | T01G1.1d.1:c.1002A>T | ||||
HGVSp | CE42645:p.Ser334= | ||||
cDNA_position | 1002 | ||||
CDS_position | 1002 | ||||
Protein_position | 334 | ||||
Exon_number | 4/4 | ||||
Codon_change | tcA/tcT | ||||
Amino_acid_change | S | ||||
F54E12.5b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F54E12.5b.1:c.414-10T>A | ||||
Intron_number | 3/4 | ||||
T01G1.1e.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | T01G1.1e.1:c.4374A>T | ||||
HGVSp | CE53084:p.Ser1458= | ||||
cDNA_position | 4447 | ||||
CDS_position | 4374 | ||||
Protein_position | 1458 | ||||
Exon_number | 20/21 | ||||
Codon_change | tcA/tcT | ||||
Amino_acid_change | S | ||||
T01G1.1a.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | T01G1.1a.1:c.4806A>T | ||||
HGVSp | CE37926:p.Ser1602= | ||||
cDNA_position | 4873 | ||||
CDS_position | 4806 | ||||
Protein_position | 1602 | ||||
Exon_number | 22/23 | ||||
Codon_change | tcA/tcT | ||||
Amino_acid_change | S | ||||
T01G1.1c.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | T01G1.1c.1:c.4731A>T | ||||
HGVSp | CE40999:p.Ser1577= | ||||
cDNA_position | 4798 | ||||
CDS_position | 4731 | ||||
Protein_position | 1577 | ||||
Exon_number | 22/23 | ||||
Codon_change | tcA/tcT | ||||
Amino_acid_change | S | ||||
F54E12.5c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F54E12.5c.1:c.381-10T>A | ||||
Intron_number | 2/3 | ||||
Remark | [20081124 db] this Variation was previously named hw59291 | ||||
Method | WGS_Hawaiian_Waterston |