WormBase Tree Display for Variation: WBVar00052997
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WBVar00052997 | Evidence | Paper_evidence | WBPaper00005369 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00052997 | |||
Other_name | CE4-188 | ||||
haw59858 | |||||
cewivar00155987 | |||||
Y55D9A.1b.1:c.487C>T | |||||
Y55D9A.1c.1:c.481C>T | |||||
CE29066:p.Pro163Ser | |||||
CE19234:p.Pro161Ser | |||||
Y55D9A.1a.1:c.481C>T | |||||
CE40826:p.Pro161Ser | |||||
HGVSg | CHROMOSOME_IV:g.12613441G>A | ||||
Sequence_details | SMap | S_parent | Sequence | Y55D9A | |
Flanking_sequences | tagccatatgtttttatcggtatgttttaatttctagaaattttataaaaacaatttttctgtttagaaaaaagggttaaaaatcaatggaaaatcgtaaaaattgtgagatttcttcttcttcttttcgaaaactttttgcatccaattaaatccagatgtttcatttttttttcgtttaaaaatttcaaaagctcaccaataaattgttcttcatcaacaaccatcacttcatcatcattttcatttg | tttcttctgattctctttttcatcagtagtcatcattacagtttcttcttcactttcctctacatcagtgctctccattcgttcaattggagctgttttaagcattcgaatagctgttggtgaagactcttctgacgtttttcgtgccaaactaccacgtctttcgatttggcttgttgaaactggaacttttagaacattggaattaaaagatagaaaattatggaaaacagttttttctaatttttta | |||
Mapping_target | Y55D9A | ||||
Type_of_mutation | Substitution | g | a | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Confirmed_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain (14) | |||||
Laboratory | RW | ||||
Person | WBPerson1562 | ||||
Analysis | SNP_Swan | ||||
Million_mutation_project_reanalysis | |||||
WGS_Hawaiian_Waterston | |||||
History | Acquires_merge | WBVar00192582 | |||
Status | Live | ||||
Affects | Gene | WBGene00013223 | |||
Transcript | Y55D9A.1c.1 | VEP_consequence | missense_variant | ||
VEP_impact | MODERATE | ||||
HGVSc | Y55D9A.1c.1:c.481C>T | ||||
HGVSp | CE40826:p.Pro161Ser | ||||
cDNA_position | 486 | ||||
CDS_position | 481 | ||||
Protein_position | 161 | ||||
Exon_number | 4/11 | ||||
Codon_change | Cca/Tca | ||||
Amino_acid_change | P/S | ||||
Y55D9A.1b.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | Y55D9A.1b.1:c.487C>T | ||||
HGVSp | CE29066:p.Pro163Ser | ||||
cDNA_position | 492 | ||||
CDS_position | 487 | ||||
Protein_position | 163 | ||||
Exon_number | 4/12 | ||||
Codon_change | Cca/Tca | ||||
Amino_acid_change | P/S | ||||
Y55D9A.1a.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | Y55D9A.1a.1:c.481C>T | ||||
HGVSp | CE19234:p.Pro161Ser | ||||
cDNA_position | 485 | ||||
CDS_position | 481 | ||||
Protein_position | 161 | ||||
Exon_number | 4/12 | ||||
Codon_change | Cca/Tca | ||||
Amino_acid_change | P/S | ||||
Reference | WBPaper00005369 | ||||
Method | SNP_Swan |