WormBase Tree Display for Variation: WBVar01447062
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WBVar01447062 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01447062 | ||||
Other_name | F10E9.8.1:c.1287+42C>A | |||||
HGVSg | CHROMOSOME_III:g.8316967G>T | |||||
Sequence_details | SMap | S_parent | Sequence | F10E9 | ||
Flanking_sequences | TTGAGAAAAATTTTCAATCGAAATTTCGTG | TTTTTCTCGAATAACTATTTCTTGCTTAAA | ||||
Mapping_target | F10E9 | |||||
Type_of_mutation | Substitution | g | t | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain (31) | ||||||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | WGS_Andersen | |||||
DB_info | Database | dbSNP_rs | rs | 193333652 | ||
dbSNP_ss | ss | 295509571 | ||||
Status | Live | |||||
Affects | Gene | WBGene00004726 | ||||
Transcript | F10E9.8.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | F10E9.8.1:c.1287+42C>A | |||||
Intron_number | 6/11 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |