WormBase Tree Display for Variation: WBVar01393743
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WBVar01393743 | Evidence | Paper_evidence | WBPaper00037807 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01393743 | ||||
Other_name | C52E12.2a.2:c.4057+36del | |||||
C52E12.2a.1:c.4057+36del | ||||||
C52E12.2b.1:c.4189+36del | ||||||
HGVSg | CHROMOSOME_II:g.7008948del | |||||
Sequence_details | SMap | S_parent | Sequence | C52E12 | ||
Flanking_sequences | ACGAGAAAGATAAAGGTGAGAATGGGTTTAACAGTAAAATACAATTATCT | CCCTCTGTCGTAAAGGTGAAGTTAGTAGGGATTTTTGTAGGAATACAGTT | ||||
Mapping_target | C52E12 | |||||
Type_of_mutation | Deletion | A | Paper_evidence | WBPaper00037807 | ||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00006642 | From_analysis | WGS_De_Bono | |||
Laboratory | AX | |||||
Analysis | WGS_De_Bono | |||||
DB_info | Database | dbSNP_ss | ss | 539113165 | ||
Status | Live | |||||
Affects | Gene | WBGene00006831 | ||||
Transcript | C52E12.2a.2 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | C52E12.2a.2:c.4057+36del | |||||
Intron_number | 20/23 | |||||
C52E12.2b.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C52E12.2b.1:c.4189+36del | |||||
Intron_number | 21/24 | |||||
C52E12.2a.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C52E12.2a.1:c.4057+36del | |||||
Intron_number | 20/23 | |||||
Reference | WBPaper00037807 | |||||
Method | WGS_De_Bono |