WormBase Tree Display for Variation: WBVar01679081
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WBVar01679081 | Name | Public_name | WBVar01679081 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00369343 | |||||||
R12H7.1a.2:c.112+137G>A | ||||||||
R12H7.1a.1:c.112+137G>A | ||||||||
HGVSg | CHROMOSOME_X:g.13212680G>A | |||||||
Sequence_details | SMap | S_parent | Sequence | R12H7 | ||||
Flanking_sequences | AATCTTCATGAATTAGTACCCATTAACCAA | GACCAAGGACTTGCTCTCCCTTTCATTTTG | ||||||
Mapping_target | R12H7 | |||||||
Source_location | 225 | CHROMOSOME_X | 13212611 | 13212611 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | A | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain (16) | ||||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006749 | ||||||
Transcript | R12H7.1a.2 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | R12H7.1a.2:c.112+137G>A | |||||||
Intron_number | 3/10 | |||||||
R12H7.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | R12H7.1a.1:c.112+137G>A | |||||||
Intron_number | 2/9 | |||||||
Method | WGS_Flibotte |