WormBase Tree Display for Variation: WBVar01641218
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WBVar01641218 | Name | Public_name | WBVar01641218 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00324509 | |||||||
M01G12.12.1:c.3691+41G>A | ||||||||
M01G12.12.2:c.3691+41G>A | ||||||||
HGVSg | CHROMOSOME_I:g.12100462C>T | |||||||
Sequence_details | SMap | S_parent | Sequence | Y47H10A | ||||
Flanking_sequences | CTAAGCGTGAGCCTAAACCTATCACTGTGC | TAAACCTAATCCTGAGCCTAAACCCAATCC | ||||||
Mapping_target | Y47H10A | |||||||
Source_location | 225 | CHROMOSOME_I | 12100453 | 12100453 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | C | T | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain (16) | ||||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00004509 | ||||||
Transcript | M01G12.12.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | M01G12.12.1:c.3691+41G>A | |||||||
Intron_number | 18/22 | |||||||
M01G12.12.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | M01G12.12.2:c.3691+41G>A | |||||||
Intron_number | 17/21 | |||||||
Method | WGS_Flibotte |