WormBase Tree Display for Variation: WBVar01363857
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WBVar01363857 | Evidence | Paper_evidence | WBPaper00037807 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | WBVar01363857 | |||||
Other_name | T22D2.1.1:c.2689-139A>T | ||||||
HGVSg | CHROMOSOME_II:g.2449524A>T | ||||||
Sequence_details | SMap | S_parent | Sequence | T22D2 | |||
Flanking_sequences | AGTTTTTGAGAAAAATTCGAAAAAAAAATTGATTTAAAAATTTTCGAAAA | ATTTTTTTTTTTTTAATTTTAATTGAGGGTTATCTCAAAAACTAGAAGTG | |||||
Mapping_target | T22D2 | ||||||
Type_of_mutation | Substitution | a | T | Paper_evidence | WBPaper00037807 | ||
SeqStatus | Sequenced | ||||||
Variation_type | SNP | ||||||
Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain | WBStrain00004602 | From_analysis | WGS_De_Bono | ||||
Laboratory | AX | ||||||
Analysis | WGS_De_Bono | ||||||
DB_info | Database | dbSNP_ss | ss | 539039235 | |||
Status | Live | ||||||
Affects | Gene | WBGene00006882 | |||||
Transcript | T22D2.1.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | ||||||
HGVSc | T22D2.1.1:c.2689-139A>T | ||||||
Intron_number | 17/19 | ||||||
Reference | WBPaper00037807 | ||||||
Method | WGS_De_Bono |