WormBase Tree Display for Variation: WBVar01309149
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WBVar01309149 | Evidence | Paper_evidence | WBPaper00037807 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | WBVar01309149 | |||||
Other_name | cewivar00508469 | ||||||
T24H10.7g.1:c.275+2808C>T | |||||||
T24H10.7f.1:c.551+2808C>T | |||||||
T24H10.7a.1:c.707+2808C>T | |||||||
T24H10.7i.1:c.398+2808C>T | |||||||
T24H10.7h.1:c.509+2808C>T | |||||||
T24H10.7b.1:c.647+2808C>T | |||||||
HGVSg | CHROMOSOME_II:g.9126144C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | T24H10 | |||
Flanking_sequences | AAAAGAGAAATGACAAATTTCCGGAGAAAAAAGAATTGCACGGCTAATGA | TCAATTTTCCCAATTCTTGACGAAAATGAAATGACTAGAATACTAACTAC | |||||
Mapping_target | T24H10 | ||||||
Type_of_mutation | Substitution | c | T | Paper_evidence | WBPaper00037807 | ||
SeqStatus | Sequenced | ||||||
Variation_type | SNP | ||||||
Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain | WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | ||||
WGS_De_Bono | |||||||
Laboratory | AX | ||||||
Analysis | WGS_De_Bono | ||||||
Million_mutation_project_reanalysis | |||||||
DB_info | Database | dbSNP_ss | ss | 539166515 | |||
Status | Live | ||||||
Affects | Gene | WBGene00012005 | |||||
Transcript | T24H10.7g.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | ||||||
HGVSc | T24H10.7g.1:c.275+2808C>T | ||||||
Intron_number | 2/3 | ||||||
T24H10.7f.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | T24H10.7f.1:c.551+2808C>T | ||||||
Intron_number | 6/8 | ||||||
T24H10.7i.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | T24H10.7i.1:c.398+2808C>T | ||||||
Intron_number | 3/4 | ||||||
T24H10.7h.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | T24H10.7h.1:c.509+2808C>T | ||||||
Intron_number | 4/5 | ||||||
T24H10.7a.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | T24H10.7a.1:c.707+2808C>T | ||||||
Intron_number | 7/9 | ||||||
T24H10.7b.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | T24H10.7b.1:c.647+2808C>T | ||||||
Intron_number | 7/9 | ||||||
Reference | WBPaper00037807 | ||||||
Method | WGS_De_Bono |