WormBase Tree Display for Variation: WBVar01471078
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WBVar01471078 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01471078 | ||||
Other_name | F13D2.1b.1:c.1198-22G>A | |||||
F13D2.1a.1:c.1198-22G>A | ||||||
HGVSg | CHROMOSOME_X:g.11174239C>T | |||||
Sequence_details | SMap | S_parent | Sequence | F13D2 | ||
Flanking_sequences | TCGGTTGGCCTAAAAGAATGCTCATTGTCT | ATTAAATTGTTTTTTGAATTAGTCAACTGC | ||||
Mapping_target | F13D2 | |||||
Type_of_mutation | Substitution | c | t | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00005835 | From_analysis | WGS_Andersen | |||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | WGS_Andersen | |||||
DB_info | Database | dbSNP_rs | rs | 193356380 | ||
dbSNP_ss | ss | 295532299 | ||||
Status | Live | |||||
Affects | Gene | WBGene00008735 | ||||
Transcript | F13D2.1b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | F13D2.1b.1:c.1198-22G>A | |||||
Intron_number | 12/38 | |||||
F13D2.1a.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F13D2.1a.1:c.1198-22G>A | |||||
Intron_number | 11/37 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |