WormBase Tree Display for Variation: WBVar01469448
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WBVar01469448 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01469448 | ||||
Other_name | cewivar00056983 | |||||
K11G12.3.1:c.909+24A>T | ||||||
HGVSg | CHROMOSOME_X:g.6717498T>A | |||||
Sequence_details | SMap | S_parent | Sequence | K11G12 | ||
Flanking_sequences | TGAATTCTCAATTAATTTTAAATTTATCAT | TGTTATCAGTTTATTTTTCTTACAACGTCA | ||||
Mapping_target | K11G12 | |||||
Type_of_mutation | Substitution | t | a | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain (115) | ||||||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | Million_mutation_project_reanalysis | |||||
WGS_Andersen | ||||||
DB_info | Database | dbSNP_rs | rs | 193354750 | ||
dbSNP_ss | ss | 295530669 | ||||
Status | Live | |||||
Affects | Gene | WBGene00004877 | ||||
Transcript | K11G12.3.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | K11G12.3.1:c.909+24A>T | |||||
Intron_number | 7/13 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |