WormBase Tree Display for Variation: WBVar01448412
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WBVar01448412 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01448412 | ||||
Other_name | C44B9.4.2:c.1276+379T>C | |||||
C44B9.4.1:c.1276+379T>C | ||||||
HGVSg | CHROMOSOME_III:g.10887261T>C | |||||
Sequence_details | SMap | S_parent | Sequence | C44B9 | ||
Flanking_sequences | TGCAATGTTTTTCTTTAAAAATCCAAAACC | ACTAATTCACCTATTTCAATCCTAAATAAT | ||||
Mapping_target | C44B9 | |||||
Type_of_mutation | Substitution | t | c | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain (73) | ||||||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | WGS_Andersen | |||||
DB_info | Database | dbSNP_rs | rs | 193334578 | ||
dbSNP_ss | ss | 295510497 | ||||
Status | Live | |||||
Affects | Gene | WBGene00008081 | ||||
Transcript | C44B9.4.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | C44B9.4.1:c.1276+379T>C | |||||
Intron_number | 7/13 | |||||
C44B9.4.2 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C44B9.4.2:c.1276+379T>C | |||||
Intron_number | 8/14 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |