WormBase Tree Display for Variation: WBVar00270509
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WBVar00270509 | Evidence | Paper_evidence | WBPaper00005369 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00270509 | |||
Other_name | uCE4-855 | ||||
cewivar00038501 | |||||
CE50613:p.Pro136Ser | |||||
F49F1.6b.1:c.406C>T | |||||
CE34873:p.Pro206Ser | |||||
F49F1.6a.1:c.616C>T | |||||
HGVSg | CHROMOSOME_IV:g.4121672G>A | ||||
Sequence_details | SMap | S_parent | Sequence | F49F1 | |
Flanking_sequences | AATTTCGAAATGAGCATCAATCTATAAACTAACTTTGGCGACGAATCCTTGCATGGTGGCTTTGGCGTAGTTGATGGAAGCTTCTTGGTCGTGGTAGCTG | CAGTTTTGTTGTAGTACTTGGTACTACTGTAGTCGTAGGCTTTACCGTAGTGAGCAACGTAGTTTGAGCCATAGGTACCCCAGTACTTCCACAAACTCCA | |||
Mapping_target | F49F1 | ||||
Type_of_mutation | Substitution | G | A | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain (25) | |||||
Analysis | SNP_Swan | ||||
Million_mutation_project_reanalysis | |||||
Status | Live | ||||
Affects | Gene | WBGene00018646 | |||
Transcript | F49F1.6b.1 | VEP_consequence | missense_variant | ||
VEP_impact | MODERATE | ||||
HGVSc | F49F1.6b.1:c.406C>T | ||||
HGVSp | CE50613:p.Pro136Ser | ||||
cDNA_position | 406 | ||||
CDS_position | 406 | ||||
Protein_position | 136 | ||||
Exon_number | 4/5 | ||||
Codon_change | Cca/Tca | ||||
Amino_acid_change | P/S | ||||
F49F1.6a.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | F49F1.6a.1:c.616C>T | ||||
HGVSp | CE34873:p.Pro206Ser | ||||
cDNA_position | 762 | ||||
CDS_position | 616 | ||||
Protein_position | 206 | ||||
Exon_number | 6/8 | ||||
Codon_change | Cca/Tca | ||||
Amino_acid_change | P/S | ||||
Reference | WBPaper00005369 | ||||
Method | SNP_Swan |