WormBase Tree Display for Variation: WBVar01552083
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WBVar01552083 | Name | Public_name | WBVar01552083 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00129190 | |||||||
F31B12.1k.1:c.5134+1482T>G | ||||||||
F31B12.1h.1:c.4984+1482T>G | ||||||||
F31B12.1a.1:c.-32T>G | ||||||||
F31B12.1g.1:c.4954+1482T>G | ||||||||
F31B12.1j.1:c.4933+1482T>G | ||||||||
F31B12.1d.1:c.5125+1482T>G | ||||||||
F31B12.1i.1:c.5104+1482T>G | ||||||||
F31B12.1l.1:c.4963+1482T>G | ||||||||
HGVSg | CHROMOSOME_X:g.10812566A>C | |||||||
Sequence_details | SMap | S_parent | Sequence | F31B12 | ||||
Flanking_sequences | GCATTTTAGGATGTATTTTGAGAAATTACA | TGGAAACTGTAATTGTCTCATATTTTGATT | ||||||
Mapping_target | F31B12 | |||||||
Source_location | 225 | CHROMOSOME_X | 10812501 | 10812501 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00004599 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00004036 | ||||||
Transcript | F31B12.1j.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1j.1:c.4933+1482T>G | |||||||
Intron_number | 34/63 | |||||||
F31B12.1h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1h.1:c.4984+1482T>G | |||||||
Intron_number | 34/63 | |||||||
F31B12.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1d.1:c.5125+1482T>G | |||||||
Intron_number | 35/64 | |||||||
F31B12.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1g.1:c.4954+1482T>G | |||||||
Intron_number | 34/63 | |||||||
F31B12.1a.1 | VEP_consequence | 5_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1a.1:c.-32T>G | |||||||
cDNA_position | 7 | |||||||
Exon_number | 1/34 | |||||||
F31B12.1l.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1l.1:c.4963+1482T>G | |||||||
Intron_number | 34/63 | |||||||
F31B12.1i.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1i.1:c.5104+1482T>G | |||||||
Intron_number | 35/64 | |||||||
F31B12.1k.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1k.1:c.5134+1482T>G | |||||||
Intron_number | 35/64 | |||||||
Method | WGS_Flibotte |