WormBase Tree Display for Variation: WBVar00002406
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WBVar00002406 | Name | Public_name | WBVar00002406 | ||
---|---|---|---|---|---|
Other_name | pas12078 | ||||
cewivar00066000 | |||||
F53G12.5b.1:c.630+1048C>T | |||||
F53G12.5a.1:c.546+1048C>T | |||||
F53G12.5a.2:c.546+1048C>T | |||||
F53G12.5a.3:c.546+1048C>T | |||||
HGVSg | CHROMOSOME_I:g.130381C>T | ||||
Sequence_details | SMap | S_parent | Sequence | F53G12 | |
Flanking_sequences | actgctgtggcaaacaaacaaaaacaatcaaacttgtgcggaattgatattctaaagagaataaagagcaaccatgggcgccgaaacgagcagcggaagggcttgtgacctcttggtgtgaattttaaacggtttccttccatccgaaatgctaaaaattcctcgggagccgtttagggtcttcactgagagatgatgattagaatcttttaatttggtagaattccccccgcgggaccgattaatgttgcatgtcgtcttcttcttcttggcagcaaaatatcattgttgatgagatat | tcagtttgatgctcaatgacgccttgagaaacatccagcacacagtagattagtcgaattaccgatggatggggccgcccgggtttttggagccaagagtcacgcgatggggagtccacatacacacgcaccaactctttcattccatctaacagggtagtagggtgaagaaaaggggggggatcgcgatgacaaagagactcaattaattaaatgaccggggcgggcgccaaattgcacatatgcttggttttattgcaccgttggctcagggagagcaacattttgtggcagcaccag | |||
Mapping_target | F53G12 | ||||
Type_of_mutation | Substitution | C | T | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain (150) | |||||
Laboratory | QX | ||||
AX | |||||
Person | WBPerson6900 | ||||
WBPerson1730 | |||||
Analysis | WGS_Pasadena_Quinlan | ||||
WGS_De_Bono | |||||
Million_mutation_project_reanalysis | |||||
WGS_Andersen | |||||
History | Acquires_merge | WBVar01417382 | |||
WBVar01429704 | |||||
WBVar01276462 | |||||
WBVar01276590 | |||||
Status | Live | ||||
Affects | Gene | WBGene00003229 | |||
Transcript | F53G12.5a.2 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | F53G12.5a.2:c.546+1048C>T | ||||
Intron_number | 6/9 | ||||
F53G12.5a.3 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F53G12.5a.3:c.546+1048C>T | ||||
Intron_number | 5/8 | ||||
F53G12.5b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F53G12.5b.1:c.630+1048C>T | ||||
Intron_number | 6/9 | ||||
F53G12.5a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F53G12.5a.1:c.546+1048C>T | ||||
Intron_number | 4/7 | ||||
Reference | WBPaper00040707 | ||||
WBPaper00037807 | |||||
Method | WGS_Pasadena_Quinlan |