WormBase Tree Display for Variation: WBVar00099905
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WBVar00099905 | Name | Public_name | WBVar00099905 | ||
---|---|---|---|---|---|
Other_name | pas4764 | ||||
cewivar00061551 | |||||
F31B12.1i.1:c.551+243A>G | |||||
F31B12.1l.1:c.551+243A>G | |||||
F31B12.1g.1:c.551+243A>G | |||||
F31B12.1h.1:c.551+243A>G | |||||
F31B12.1d.1:c.551+243A>G | |||||
F31B12.1k.1:c.551+243A>G | |||||
F31B12.1j.1:c.551+243A>G | |||||
HGVSg | CHROMOSOME_X:g.10829585T>C | ||||
Sequence_details | SMap | S_parent | Sequence | C05A9 | |
Flanking_sequences | gctaccccattatattatggtcttgaacactgatgtacgtaggaaaatacacatttcataagaggaattaaaggtccaacaatttttaaatattttgtgttgtgaactgcactaatatttaaagcttaaataaattcactaaaacaaaagttttgaataattcagtacacatccgcgttttgtttttgacaactactgaatgtctgaaaagttcacttttttaaaggtgcaatttttgcacgacaacacatatagaaaatacatggttcaaattatagcttcagaaactaaaactaaaat | aattatagatatatacttgaacaaaaataaaaatggttttctaattactttgtgatgggtttttctgaaattcaacttaaacataaaaacgtctcaaagtgaatacaaaatttgacttgactctcgcaagtcctttctaacagcatatgtgacgcacaattttgatctgagttttcagtttcttggccggatttctcatgaataaattgtttccgagtatctacatataaacatgaccccaccttcctccggaatgtgtggacaccgtactactggcattggaacgtcggtgtgcccccg | |||
Mapping_target | C05A9 | ||||
Type_of_mutation | Substitution | T | C | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain (18) | |||||
Person | WBPerson6900 | ||||
Analysis | WGS_Pasadena_Quinlan | ||||
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.551+243A>G | ||||
Intron_number | 7/63 | ||||
F31B12.1g.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F31B12.1g.1:c.551+243A>G | ||||
Intron_number | 7/63 | ||||
F31B12.1d.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F31B12.1d.1:c.551+243A>G | ||||
Intron_number | 7/64 | ||||
F31B12.1h.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F31B12.1h.1:c.551+243A>G | ||||
Intron_number | 7/63 | ||||
F31B12.1l.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F31B12.1l.1:c.551+243A>G | ||||
Intron_number | 7/63 | ||||
F31B12.1i.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F31B12.1i.1:c.551+243A>G | ||||
Intron_number | 7/64 | ||||
F31B12.1k.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F31B12.1k.1:c.551+243A>G | ||||
Intron_number | 7/64 | ||||
Method | WGS_Pasadena_Quinlan |