WormBase Tree Display for Variation: WBVar00904934
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| WBVar00904934 | Name | Public_name | gk442970 | ||
|---|---|---|---|---|---|
| Other_name | M01H9.3b.2:c.-215A>T | ||||
| M01H9.3b.1:c.-1-214A>T | |||||
| M01H9.3a.1:c.183-214A>T | |||||
| M01H9.3c.1:c.30-214A>T | |||||
| M01H9.3e.1:c.-215A>T | |||||
| HGVSg | CHROMOSOME_IV:g.4470056T>A | ||||
| Sequence_details | SMap | S_parent | Sequence | M01H9 | |
| Flanking_sequences | TTTTTAAGGCGAGATAGGGGGTGGGAGAGAGAAAGCTCTCTACTCGCATG | GACCACGTGAATTTGCACATGCGCGCGCGCGCCCAGTGCCTCAACCCGTA | |||
| Mapping_target | M01H9 | ||||
| Type_of_mutation | Substitution | T | A | ||
| SeqStatus | Sequenced | ||||
| Variation_type | Allele | ||||
| Origin | Species | Caenorhabditis elegans | |||
| Strain | WBStrain00038954 | ||||
| Laboratory | VC | ||||
| Analysis | Million_Mutation_Project | ||||
| Status | Live | ||||
| Affects | Gene | WBGene00019719 | |||
| Transcript | M01H9.3b.2 | VEP_consequence | 5_prime_UTR_variant | ||
| VEP_impact | MODIFIER | ||||
| HGVSc | M01H9.3b.2:c.-215A>T | ||||
| cDNA_position | 3 | ||||
| Exon_number | 1/6 | ||||
| M01H9.3a.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | M01H9.3a.1:c.183-214A>T | ||||
| Intron_number | 3/7 | ||||
| M01H9.3e.1 | VEP_consequence | 5_prime_UTR_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | M01H9.3e.1:c.-215A>T | ||||
| cDNA_position | 771 | ||||
| Exon_number | 1/6 | ||||
| M01H9.3c.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | M01H9.3c.1:c.30-214A>T | ||||
| Intron_number | 2/6 | ||||
| M01H9.3b.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | M01H9.3b.1:c.-1-214A>T | ||||
| Intron_number | 1/6 | ||||
| Reference | WBPaper00042537 | ||||
| Method | Million_mutation |
