WormBase Tree Display for Variation: WBVar00089147
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WBVar00089147 | Evidence | Paper_evidence | WBPaper00026601 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | mn396 | |||||
Other_name | C27H5.7b.1:c.988-1G>A | ||||||
C27H5.7a.1:c.1054-1G>A | |||||||
HGVSg | CHROMOSOME_II:g.7169755C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | C27H5 | |||
Flanking_sequences | tatttttgtagaaattttttttttatttca | agagaacacctgaagattgctgaaaatttc | |||||
Mapping_target | C27H5 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00026601 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain | WBStrain00034376 | ||||||
Laboratory | SP | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00001129 | |||||
Transcript | C27H5.7a.1 | VEP_consequence | splice_acceptor_variant | ||||
VEP_impact | HIGH | ||||||
HGVSc | C27H5.7a.1:c.1054-1G>A | ||||||
Intron_number | 8/13 | ||||||
C27H5.7b.1 | VEP_consequence | splice_acceptor_variant | |||||
VEP_impact | HIGH | ||||||
HGVSc | C27H5.7b.1:c.988-1G>A | ||||||
Intron_number | 8/12 | ||||||
Interactor | WBInteraction000520978 | ||||||
Genetics | Interpolated_map_position | II | 0.496688 | ||||
Mapping_data | In_2_point | 7008 | |||||
In_multi_point | 3048 | ||||||
3049 | |||||||
3050 | |||||||
3051 | |||||||
3052 | |||||||
In_pos_neg_data | 8312 | ||||||
8313 | |||||||
8314 | |||||||
8315 | |||||||
Description | Phenotype (13) | ||||||
Phenotype_not_observed | WBPhenotype:0000398 | Paper_evidence | WBPaper00002087 | ||||
Curator_confirmed | WBPerson48 | ||||||
WBPhenotype:0000646 | Paper_evidence | WBPaper00002087 | |||||
Curator_confirmed | WBPerson48 | ||||||
Remark | Normal mobility when prodded. | Paper_evidence | WBPaper00002087 | ||||
Curator_confirmed | WBPerson48 | ||||||
Reference | WBPaper00026666 | ||||||
WBPaper00029016 | |||||||
WBPaper00002087 | |||||||
WBPaper00026601 | |||||||
WBPaper00026371 | |||||||
WBPaper00055368 | |||||||
Method | Substitution_allele |