WormBase Tree Display for Variation: WBVar01450654
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WBVar01450654 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01450654 | ||||
Other_name | cewivar00379043 | |||||
Y104H12A.1c.1:c.48+2582T>A | ||||||
Y104H12A.1a.1:c.354+2582T>A | ||||||
Y104H12A.1b.1:c.150+2582T>A | ||||||
HGVSg | CHROMOSOME_IV:g.1391285T>A | |||||
Sequence_details | SMap | S_parent | Sequence | Y77E11A | ||
Flanking_sequences | TGACACACAACCGACGGTGACTAATATTTA | ATACGTGTCGGAATTCTTCTCGGTTTTTTG | ||||
Mapping_target | Y77E11A | |||||
Type_of_mutation | Substitution | t | a | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00006618 | From_analysis | WGS_Andersen | |||
WBStrain00006632 | From_analysis | WGS_Andersen | ||||
WBStrain00006640 | From_analysis | Million_mutation_project_reanalysis | ||||
WGS_Andersen | ||||||
WBStrain00022878 | From_analysis | Million_mutation_project_reanalysis | ||||
WGS_Andersen | ||||||
WBStrain00022879 | From_analysis | WGS_Andersen | ||||
WBStrain00022880 | From_analysis | WGS_Andersen | ||||
WBStrain00022885 | From_analysis | WGS_Andersen | ||||
WBStrain00022911 | From_analysis | WGS_Andersen | ||||
WBStrain00023079 | From_analysis | WGS_Andersen | ||||
WBStrain00023665 | From_analysis | Million_mutation_project_reanalysis | ||||
WGS_Andersen | ||||||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | Million_mutation_project_reanalysis | |||||
WGS_Andersen | ||||||
DB_info | Database | dbSNP_rs | rs | 193336311 | ||
dbSNP_ss | ss | 295512230 | ||||
Status | Live | |||||
Affects | Gene | WBGene00022423 | ||||
Transcript | Y104H12A.1a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | Y104H12A.1a.1:c.354+2582T>A | |||||
Intron_number | 5/11 | |||||
Y104H12A.1b.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | Y104H12A.1b.1:c.150+2582T>A | |||||
Intron_number | 2/7 | |||||
Y104H12A.1c.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | Y104H12A.1c.1:c.48+2582T>A | |||||
Intron_number | 1/6 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |