WormBase Tree Display for Variation: WBVar00104560
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WBVar00104560 | Name | Public_name | WBVar00104560 | ||
---|---|---|---|---|---|
Other_name | pas9419 | ||||
haw26267 | |||||
haw131285 | |||||
cewivar00091316 | |||||
C52E12.2a.1:c.2345+779A>C | |||||
C52E12.2a.2:c.2345+779A>C | |||||
C52E12.2b.1:c.2346-407A>C | |||||
HGVSg | CHROMOSOME_II:g.7005569A>C | ||||
Sequence_details | SMap | S_parent | Sequence | C52E12 | |
Flanking_sequences | gaaattttgtttccaaagtggttgcctataactcagttcccctcctacaatttttttaaagactgttctgaagtttttaaactaaaaacagagttttgaacttctcaacccttgaatatatatttttcaaaaattaagttttttttggaaaattaagtttttttttggattttggacgtttaaattttaaaaaaaattgaatttctcactaccagagtcaattttaaaaatatggtttttaatacatttttcaaacttttaaaatttttacatttttgcgaatacttatcgaagaatctc | aatggaaagttgttggtaattatccggcgtactaaaaattcccggttgtttaactttggcttgtcaacaacaagtttacaacgaattccaaaacaacttatatattcgtttattcataaatctagagagaaaaaataaataataaccggagagtaattggtgcgagggaataaaggaatttaaaatataaactaccttctagagtagttttcaaattgttttgatttttttttgcaaattcaaaacgagataatcgaatttagacaatggggtgtggcgcacgccccgtcgaacgtctaa | |||
Mapping_target | C52E12 | ||||
Type_of_mutation | Substitution | A | C | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain (162) | |||||
Laboratory | QX | ||||
AX | |||||
RW | |||||
Person | WBPerson6900 | ||||
WBPerson4037 | |||||
WBPerson1730 | |||||
WBPerson1562 | |||||
Analysis | WGS_Pasadena_Quinlan | ||||
WGS_De_Bono | |||||
WGS_Yanai | |||||
Million_mutation_project_reanalysis | |||||
WGS_Hawaiian_Waterston | |||||
WGS_Andersen | |||||
History | Acquires_merge | WBVar00173017 | |||
WBVar01307358 | |||||
WBVar01373018 | |||||
WBVar00551150 | |||||
WBVar01240980 | |||||
WBVar01438343 | |||||
Status | Live | ||||
Affects | Gene | WBGene00006831 | |||
Transcript | C52E12.2a.2 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | C52E12.2a.2:c.2345+779A>C | ||||
Intron_number | 13/23 | ||||
C52E12.2b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C52E12.2b.1:c.2346-407A>C | ||||
Intron_number | 13/24 | ||||
C52E12.2a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C52E12.2a.1:c.2345+779A>C | ||||
Intron_number | 13/23 | ||||
Reference | WBPaper00038208 | ||||
WBPaper00040707 | |||||
WBPaper00037807 | |||||
Method | WGS_Pasadena_Quinlan |