WormBase Tree Display for Variation: WBVar00038261
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WBVar00038261 | Name | Public_name | WBVar00038261 | ||
---|---|---|---|---|---|
Other_name | pas19249 | ||||
cewivar00080049 | |||||
F56D12.1b.1:c.*547C>T | |||||
CE29047:p.Leu506= | |||||
CE40074:p.Leu366= | |||||
F56D12.1d.1:c.1098C>T | |||||
F56D12.1a.2:c.1518C>T | |||||
F56D12.1a.1:c.1518C>T | |||||
HGVSg | CHROMOSOME_II:g.1306559G>A | ||||
Sequence_details | SMap | S_parent | Sequence | Y57G7A | |
Flanking_sequences | ttatgcgatcacgggggaaaaaaaattaaaattcagtggtaaagcaataattgttgacctaatcaaaaagaaaactatattctcaatatgagaaaaatcggaaatgaaaagaaaaaaacaacataattattccattgatggatatttccagtcagtcaatgacaccgacgtctccttaatcgtcagcggcgaggtccatcggagcccatagtgggggccaccggccttatcattggttccggacaatctggagcctccgaatggctgctggccgacgattgatccagttgatttgtcgtt | aggtacatgttgccgacggcgtcgcggagaacatcgcgagctctgagaaaaaaaaacactttgttgaaaaacgtttttaacacaaaaattcgcctcaaaaatctcgaaaaatcgatcgaaatccaacaaaaattccaataaaaaataccgtagccctttaaagggacacacactttcactgttgggtctcgccacgctcaggaacatcttactgtcgctttcaaattttttgtttgttgttatcgcttttttttttcgatttttgccagtttttctagcttttcatttgatttgtgacga | |||
Mapping_target | Y57G7A | ||||
Type_of_mutation | Substitution | G | A | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00000034 | From_analysis | Million_mutation_project_reanalysis | ||
WBStrain00004599 | From_analysis | Million_mutation_project_reanalysis | |||
WBStrain00004604 | From_analysis | WGS_Pasadena_Quinlan | |||
WBStrain00006625 | From_analysis | Million_mutation_project_reanalysis | |||
WBStrain00023665 | From_analysis | Million_mutation_project_reanalysis | |||
WBStrain00027652 | From_analysis | Million_mutation_project_reanalysis | |||
Person | WBPerson6900 | ||||
Analysis | WGS_Pasadena_Quinlan | ||||
Million_mutation_project_reanalysis | |||||
Status | Live | ||||
Affects | Gene | WBGene00000112 | |||
Transcript | F56D12.1b.1 | VEP_consequence | 3_prime_UTR_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | F56D12.1b.1:c.*547C>T | ||||
cDNA_position | 2088 | ||||
Exon_number | 8/8 | ||||
F56D12.1a.2 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | F56D12.1a.2:c.1518C>T | ||||
HGVSp | CE29047:p.Leu506= | ||||
cDNA_position | 1617 | ||||
CDS_position | 1518 | ||||
Protein_position | 506 | ||||
Exon_number | 9/10 | ||||
Codon_change | ctC/ctT | ||||
Amino_acid_change | L | ||||
F56D12.1a.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | F56D12.1a.1:c.1518C>T | ||||
HGVSp | CE29047:p.Leu506= | ||||
cDNA_position | 1521 | ||||
CDS_position | 1518 | ||||
Protein_position | 506 | ||||
Exon_number | 8/9 | ||||
Codon_change | ctC/ctT | ||||
Amino_acid_change | L | ||||
F56D12.1d.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | F56D12.1d.1:c.1098C>T | ||||
HGVSp | CE40074:p.Leu366= | ||||
cDNA_position | 1098 | ||||
CDS_position | 1098 | ||||
Protein_position | 366 | ||||
Exon_number | 4/4 | ||||
Codon_change | ctC/ctT | ||||
Amino_acid_change | L | ||||
Method | WGS_Pasadena_Quinlan |