WormBase Tree Display for Variation: WBVar01710587
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WBVar01710587 | Name | Public_name | WBVar01710587 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00408240 | |||||||
C07A12.7b.1:c.586-69T>C | ||||||||
C07A12.7a.1:c.688-69T>C | ||||||||
C07A12.7c.2:c.-204-69T>C | ||||||||
C07A12.7c.1:c.-273T>C | ||||||||
C07A12.7a.2:c.688-69T>C | ||||||||
HGVSg | CHROMOSOME_X:g.4518754A>G | |||||||
Sequence_details | SMap | S_parent | Sequence | C07A12 | ||||
Flanking_sequences | AAACAAACAAACTTTGTAATGAAACTTTTC | AAATTTTTCAGAAATGTTTCATGACGGTTC | ||||||
Mapping_target | C07A12 | |||||||
Source_location | 225 | CHROMOSOME_X | 4518726 | 4518726 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | G | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022878 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022902 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023138 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023139 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027648 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027660 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00015561 | ||||||
Transcript | C07A12.7c.1 | VEP_consequence | 5_prime_UTR_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | C07A12.7c.1:c.-273T>C | |||||||
cDNA_position | 1288 | |||||||
Exon_number | 4/9 | |||||||
C07A12.7a.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C07A12.7a.2:c.688-69T>C | |||||||
Intron_number | 6/10 | |||||||
C07A12.7c.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C07A12.7c.2:c.-204-69T>C | |||||||
Intron_number | 3/8 | |||||||
C07A12.7b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C07A12.7b.1:c.586-69T>C | |||||||
Intron_number | 4/8 | |||||||
C07A12.7a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C07A12.7a.1:c.688-69T>C | |||||||
Intron_number | 5/9 | |||||||
Method | WGS_Flibotte |