WormBase Tree Display for Variation: WBVar00062059
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WBVar00062059 | Name | Public_name | WBVar00062059 | ||
---|---|---|---|---|---|
Other_name (14) | |||||
HGVSg | CHROMOSOME_III:g.7984909G>A | ||||
Sequence_details | SMap | S_parent | Sequence | C06G4 | |
Flanking_sequences | taatccatggggaaatgaacaggaatggaatggaccatggtcagacaattcacgcgaatggcgaagtgttccagattctgtaaaacaagatatgggactgaaattcgatcatgatggagagttttggatgtcatttgatgattttatgaggaatttcgagaaaatggaaatttgcaatcttggaccagatgttatggatgaagtctatcaaatgactggtgtcaaggccgctggaatggtttgggctgcaaatactcatgatggtgcatgggttagaaatcaaacagctggaggatgcag | aattacatcagtaagtaaatattcatctacaaatattttcaattttcaattcagacactttcgccaacaatccacaattccgagttcaacttaccgattcggatcctgatgatgatgatgaactctgcactgtaatattcgccgttttgcaaaaatacaggtagcgccaccagatagggaaatcatttttatttttccaatttttaagacgtaatctgaaacaagatggacttgacaacgtgccaattggatttgctgtctatgacgtgagactattgttattttgaagaaaaaacagga | |||
Mapping_target | C06G4 | ||||
Type_of_mutation | Substitution | G | A | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin (7) | |||||
Affects | Gene | WBGene00000542 | |||
Transcript | C06G4.2d.1 | VEP_consequence | synonymous_variant | ||
VEP_impact | LOW | ||||
HGVSc | C06G4.2d.1:c.1887G>A | ||||
HGVSp | CE30486:p.Arg629= | ||||
cDNA_position | 1887 | ||||
CDS_position | 1887 | ||||
Protein_position | 629 | ||||
Exon_number | 9/15 | ||||
Codon_change | agG/agA | ||||
Amino_acid_change | R | ||||
C06G4.2a.2 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | C06G4.2a.2:c.1950G>A | ||||
HGVSp | CE37743:p.Arg650= | ||||
cDNA_position | 2120 | ||||
CDS_position | 1950 | ||||
Protein_position | 650 | ||||
Exon_number | 11/17 | ||||
Codon_change | agG/agA | ||||
Amino_acid_change | R | ||||
C06G4.2c.1 | VEP_consequence | 3_prime_UTR_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C06G4.2c.1:c.*1792G>A | ||||
cDNA_position | 2223 | ||||
Exon_number | 10/15 | ||||
C06G4.2b.2 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | C06G4.2b.2:c.1812G>A | ||||
HGVSp | CE37744:p.Arg604= | ||||
cDNA_position | 1907 | ||||
CDS_position | 1812 | ||||
Protein_position | 604 | ||||
Exon_number | 9/17 | ||||
Codon_change | agG/agA | ||||
Amino_acid_change | R | ||||
C06G4.2a.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | C06G4.2a.1:c.1950G>A | ||||
HGVSp | CE37743:p.Arg650= | ||||
cDNA_position | 2045 | ||||
CDS_position | 1950 | ||||
Protein_position | 650 | ||||
Exon_number | 10/16 | ||||
Codon_change | agG/agA | ||||
Amino_acid_change | R | ||||
C06G4.2b.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | C06G4.2b.1:c.1812G>A | ||||
HGVSp | CE37744:p.Arg604= | ||||
cDNA_position | 1907 | ||||
CDS_position | 1812 | ||||
Protein_position | 604 | ||||
Exon_number | 9/16 | ||||
Codon_change | agG/agA | ||||
Amino_acid_change | R | ||||
Reference | WBPaper00038208 | ||||
WBPaper00004703 | |||||
WBPaper00037807 | |||||
Method | WGS_Pasadena_Quinlan |