WormBase Tree Display for Variation: WBVar01441210
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WBVar01441210 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01441210 | ||||
Other_name | Y38F1A.2.1:c.576+398G>C | |||||
HGVSg | CHROMOSOME_II:g.12956921G>C | |||||
Sequence_details | SMap | S_parent | Sequence | Y38F1A | ||
Flanking_sequences | TTTTGCCGAATATGCCGTTTGCCGAGCTTG | CAAATTTGCCGTTTGCCGAGCTTGGCGAAT | ||||
Mapping_target | Y38F1A | |||||
Type_of_mutation | Substitution | g | c | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain (54) | ||||||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | WGS_Andersen | |||||
DB_info | Database | dbSNP_rs | rs | 193328835 | ||
dbSNP_ss | ss | 295504754 | ||||
Status | Live | |||||
Affects | Gene | WBGene00012606 | ||||
Transcript | Y38F1A.2.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | Y38F1A.2.1:c.576+398G>C | |||||
Intron_number | 7/9 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |