WormBase Tree Display for Variation: WBVar02136144
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WBVar02136144 | Evidence | Paper_evidence | WBPaper00045317 | |||
---|---|---|---|---|---|---|
Name | Public_name | h16705 | ||||
Other_name | C17E7.8b.1:c.190+1063G>A | |||||
C17E7.8a.1:c.190+1063G>A | ||||||
HGVSg | CHROMOSOME_V:g.3884798C>T | |||||
Sequence_details | SMap | S_parent | Sequence | C17E7 | ||
Flanking_sequences | CTAACGTGTCTACGCACACCGTCTGCCCAGACTGATCATA | GAAAATTCGGAGATGTGCAGAACGGGAAAACAACTTTTCT | ||||
Mapping_target | CHROMOSOME_V | |||||
Source_location | 200 | CHROMOSOME_V | 3884783 | 3884783 | ||
Type_of_mutation | Substitution | C | T | |||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00023759 | |||||
Laboratory | KR | |||||
Analysis | WGS_Rose | |||||
Status | Live | |||||
Affects | Gene | WBGene00003714 | ||||
Transcript | C17E7.8a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | C17E7.8a.1:c.190+1063G>A | |||||
Intron_number | 3/7 | |||||
C17E7.8b.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C17E7.8b.1:c.190+1063G>A | |||||
Intron_number | 2/6 | |||||
Reference | WBPaper00040589 | |||||
WBPaper00000975 | ||||||
WBPaper00003985 | ||||||
WBPaper00000699 | ||||||
WBPaper00045317 | ||||||
Method | WGS_Rose |