WormBase Tree Display for Variation: WBVar01452702
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WBVar01452702 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01452702 | ||||
Other_name | C11D2.6o.1:c.80-2664A>G | |||||
C11D2.6k.1:c.26-2664A>G | ||||||
C11D2.6m.1:c.80-2664A>G | ||||||
C11D2.6j.1:c.26-2664A>G | ||||||
C11D2.6p.1:c.80-2664A>G | ||||||
C11D2.6n.1:c.80-2664A>G | ||||||
C11D2.6i.1:c.26-2664A>G | ||||||
C11D2.6l.1:c.26-2664A>G | ||||||
HGVSg | CHROMOSOME_IV:g.6174070T>C | |||||
Sequence_details | SMap | S_parent | Sequence | C11D2 | ||
Flanking_sequences | AGTTTTATTCGGTTAACAAATGACGTATTG | GGACTGGAACTTTCGTCATGCGCACATCGT | ||||
Mapping_target | C11D2 | |||||
Type_of_mutation | Substitution | t | c | |||
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 | 193338359 | ||
dbSNP_ss | ss | 295514278 | ||||
Status | Live | |||||
Affects | Gene | WBGene00006809 | ||||
Transcript | C11D2.6o.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | C11D2.6o.1:c.80-2664A>G | |||||
Intron_number | 2/28 | |||||
C11D2.6p.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C11D2.6p.1:c.80-2664A>G | |||||
Intron_number | 2/28 | |||||
C11D2.6i.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C11D2.6i.1:c.26-2664A>G | |||||
Intron_number | 1/28 | |||||
C11D2.6l.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C11D2.6l.1:c.26-2664A>G | |||||
Intron_number | 1/27 | |||||
C11D2.6n.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C11D2.6n.1:c.80-2664A>G | |||||
Intron_number | 2/27 | |||||
C11D2.6j.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C11D2.6j.1:c.26-2664A>G | |||||
Intron_number | 1/26 | |||||
C11D2.6m.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C11D2.6m.1:c.80-2664A>G | |||||
Intron_number | 2/29 | |||||
C11D2.6k.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C11D2.6k.1:c.26-2664A>G | |||||
Intron_number | 1/27 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |