WormBase Tree Display for Variation: WBVar00022361
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WBVar00022361 | Evidence | Paper_evidence | WBPaper00037807 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00022361 | |||
Other_name | pas16069 | ||||
cewivar00022507 | |||||
F53A3.4d.3:c.39-312G>A | |||||
F53A3.4d.1:c.39-312G>A | |||||
F53A3.4d.2:c.39-312G>A | |||||
F53A3.4b.1:c.4905-312G>A | |||||
F53A3.4a.1:c.4800-312G>A | |||||
HGVSg | CHROMOSOME_III:g.1933872G>A | ||||
Sequence_details | SMap | S_parent | Sequence | F53A3 | |
Flanking_sequences | ttttggctgaatttgtgtcaaaattcacttttttttttactgaaaattcgaattttccccctaaaaatcgatatttcccctgtgacttgtgcgtttctcagatttttggcataaaaactgtatttattcacattttcagccttaaattggctgaaaatgtgaataaataccgtatttctgccaacaatttgacaatagagcacatttgtcactcggagatgcggaacctatgcccaaattttcatttttacggaaaacttgtgattttcacagattttcagtcgaaaatgattttagtgt | atttttgttgcgaaatctcgatttttcaatgtcattttcgaactctccacacaatttcaccccaaaatcaagttttcccggctttctagctttaaatttgaattcccgggggtactgtagccccaaaagtacgcaaacacggagcatcccacgacaaaatgcacagttttctgaaattttgcaaaaatgtgcaaattaggggtaaaatggtgctctgaattcgaatttcgcactgaaaaatcgtgaaaatgcctagtttttgagttttcctataaaaaatttgaaagttttcaaaatttg | |||
Mapping_target | F53A3 | ||||
Type_of_mutation | Substitution | G | A | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain (18) | |||||
Laboratory | AX | ||||
Person | WBPerson6900 | ||||
Analysis | WGS_Pasadena_Quinlan | ||||
WGS_De_Bono | |||||
Million_mutation_project_reanalysis | |||||
History | Acquires_merge | WBVar01326443 | |||
Status | Live | ||||
Affects | Gene | WBGene00004128 | |||
Transcript | F53A3.4d.2 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | F53A3.4d.2:c.39-312G>A | ||||
Intron_number | 6/10 | ||||
F53A3.4d.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F53A3.4d.1:c.39-312G>A | ||||
Intron_number | 7/11 | ||||
F53A3.4b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F53A3.4b.1:c.4905-312G>A | ||||
Intron_number | 19/23 | ||||
F53A3.4a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F53A3.4a.1:c.4800-312G>A | ||||
Intron_number | 19/23 | ||||
F53A3.4d.3 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F53A3.4d.3:c.39-312G>A | ||||
Intron_number | 6/10 | ||||
Reference | WBPaper00037807 | ||||
Method | WGS_Pasadena_Quinlan |