WormBase Tree Display for Variation: WBVar01820520
expand all nodes | collapse all nodes | view schema
WBVar01820520 | Name | Public_name | WBVar01820520 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00532178 | |||||||
T05A10.1m.1:c.*498C>G | ||||||||
T05A10.1j.2:c.*2322C>G | ||||||||
T05A10.1e.1:c.*498C>G | ||||||||
T05A10.1j.3:c.*2117C>G | ||||||||
T05A10.1a.1:c.*498C>G | ||||||||
T05A10.1c.1:c.*498C>G | ||||||||
T05A10.1j.1:c.*2513C>G | ||||||||
T05A10.1j.4:c.*2325C>G | ||||||||
T05A10.1h.1:c.*1183C>G | ||||||||
HGVSg | CHROMOSOME_X:g.10782884C>G | |||||||
Sequence_details | SMap | S_parent | Sequence | T05A10 | ||||
Flanking_sequences | ACATGCAATCATTTCTTGTGTCAGTATGCT | TCTAGTTTTGATTTATATTTTTGGAAATAC | ||||||
Mapping_target | T05A10 | |||||||
Source_location | 225 | CHROMOSOME_X | 10782819 | 10782819 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | C | G | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022852 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022856 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00004862 | ||||||
Transcript | T05A10.1m.1 | VEP_consequence | 3_prime_UTR_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1m.1:c.*498C>G | |||||||
cDNA_position | 6681 | |||||||
Exon_number | 27/27 | |||||||
T05A10.1j.4 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1j.4:c.*2325C>G | |||||||
cDNA_position | 6855 | |||||||
Exon_number | 27/27 | |||||||
T05A10.1j.3 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1j.3:c.*2117C>G | |||||||
cDNA_position | 6647 | |||||||
Exon_number | 26/26 | |||||||
T05A10.1j.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1j.1:c.*2513C>G | |||||||
cDNA_position | 7043 | |||||||
Exon_number | 25/25 | |||||||
T05A10.1e.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1e.1:c.*498C>G | |||||||
cDNA_position | 7128 | |||||||
Exon_number | 27/27 | |||||||
T05A10.1j.2 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1j.2:c.*2322C>G | |||||||
cDNA_position | 6852 | |||||||
Exon_number | 27/27 | |||||||
T05A10.1a.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1a.1:c.*498C>G | |||||||
cDNA_position | 6699 | |||||||
Exon_number | 24/24 | |||||||
T05A10.1c.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1c.1:c.*498C>G | |||||||
cDNA_position | 7308 | |||||||
Exon_number | 28/28 | |||||||
T05A10.1h.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1h.1:c.*1183C>G | |||||||
cDNA_position | 5861 | |||||||
Exon_number | 24/24 | |||||||
Method | WGS_Flibotte |