WormBase Tree Display for Variation: WBVar01431992
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WBVar01431992 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01431992 | ||||
Other_name | C48B6.6b.1:c.4353+20A>T | |||||
C48B6.6a.1:c.4347+20A>T | ||||||
HGVSg | CHROMOSOME_I:g.6905935T>A | |||||
Sequence_details | SMap | S_parent | Sequence | C48B6 | ||
Flanking_sequences | AAAAAATTATCAAATTTTGAGATATTCTGA | ATATTTAGATTGATCTCACCGAGTACGGTA | ||||
Mapping_target | C48B6 | |||||
Type_of_mutation | Substitution | t | a | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00031279 | From_analysis | WGS_Andersen | |||
WBStrain00031284 | From_analysis | WGS_Andersen | ||||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | WGS_Andersen | |||||
DB_info | Database | dbSNP_rs | rs | 193320055 | ||
dbSNP_ss | ss | 295495972 | ||||
Status | Live | |||||
Affects | Gene | WBGene00004879 | ||||
Transcript | C48B6.6b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | C48B6.6b.1:c.4353+20A>T | |||||
Intron_number | 26/41 | |||||
C48B6.6a.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C48B6.6a.1:c.4347+20A>T | |||||
Intron_number | 27/43 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |