WormBase Tree Display for Variation: WBVar02132510
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WBVar02132510 | Evidence | Paper_evidence | WBPaper00045317 | |||
---|---|---|---|---|---|---|
Name | Public_name | h5962 | ||||
Other_name | C38C10.5a.1:c.3382-798C>T | |||||
C38C10.5b.1:c.3400-798C>T | ||||||
HGVSg | CHROMOSOME_III:g.9402283C>T | |||||
Sequence_details | SMap | S_parent | Sequence | C38C10 | ||
Flanking_sequences | GAAGTGTTTTGAGCAAAACGCTAAAAATATTTTAAGGACC | CCTCTGGGTTTTTAATTCTTGAAATTTTATAGAATATGTG | ||||
Mapping_target | CHROMOSOME_III | |||||
Source_location | 200 | CHROMOSOME_III | 9402184 | 9402184 | ||
Type_of_mutation | Substitution | C | T | |||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00023685 | |||||
Laboratory | KR | |||||
Analysis | WGS_Rose | |||||
Status | Live | |||||
Affects | Gene | WBGene00004343 | ||||
Transcript | C38C10.5a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | C38C10.5a.1:c.3382-798C>T | |||||
Intron_number | 12/16 | |||||
C38C10.5b.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C38C10.5b.1:c.3400-798C>T | |||||
Intron_number | 11/14 | |||||
Reference | WBPaper00040589 | |||||
WBPaper00000975 | ||||||
WBPaper00003985 | ||||||
WBPaper00000699 | ||||||
WBPaper00045317 | ||||||
Method | WGS_Rose |