WormBase Tree Display for Variation: WBVar00000499
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WBVar00000499 | Evidence | Person_evidence | WBPerson616 | ||
---|---|---|---|---|---|
Name | Public_name | bn121 | |||
Other_name (4) | |||||
HGVSg | CHROMOSOME_I:g.507464_507648del | ||||
Sequence_details | SMap | S_parent | Sequence | Y65B4BL | |
Flanking_sequences | TTGACAATTTGATTTTGCAGGTCATCAAGA | TATGAGCTTCAGCCAGTTCCACTTCTCAGAC | |||
Mapping_target | Y65B4BL | ||||
Type_of_mutation | Deletion | ||||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00034459 | ||||
Laboratory | SS | ||||
Status | Live | ||||
Affects | Gene | WBGene00022034 | |||
Transcript | Y65B4BL.2a.1 | VEP_consequence | frameshift_variant | ||
VEP_impact | HIGH | ||||
HGVSc | Y65B4BL.2a.1:c.737_921del | ||||
HGVSp | CE25536:p.Met246IlefsTer2 | ||||
cDNA_position | 741-925 | ||||
CDS_position | 737-921 | ||||
Protein_position | 246-307 | ||||
Exon_number | 7/14 | ||||
Codon_change | aTGCAGCTTGGCCTGTATGTCGGCGAACGCCTACTGATTTGCAAAGAACTCTCGCAGTTCGACTTTATTATCCCACTGCAGAAGCCATTTTCCCGAGGAACGGACAAGACTTTGATCTACCCAGCCGTCGGAGAATACTTTCATTTCAGTGCTATTTGGTCGATGCAGCACAACGGTTTTCTGATC/a | ||||
Amino_acid_change | MQLGLYVGERLLICKELSQFDFIIPLQKPFSRGTDKTLIYPAVGEYFHFSAIWSMQHNGFLI/X | ||||
Y65B4BL.2b.1 | VEP_consequence | frameshift_variant | |||
VEP_impact | HIGH | ||||
HGVSc | Y65B4BL.2b.1:c.602_786del | ||||
HGVSp | CE49430:p.Met201IlefsTer2 | ||||
cDNA_position | 602-786 | ||||
CDS_position | 602-786 | ||||
Protein_position | 201-262 | ||||
Exon_number | 5/11 | ||||
Codon_change | aTGCAGCTTGGCCTGTATGTCGGCGAACGCCTACTGATTTGCAAAGAACTCTCGCAGTTCGACTTTATTATCCCACTGCAGAAGCCATTTTCCCGAGGAACGGACAAGACTTTGATCTACCCAGCCGTCGGAGAATACTTTCATTTCAGTGCTATTTGGTCGATGCAGCACAACGGTTTTCTGATC/a | ||||
Amino_acid_change | MQLGLYVGERLLICKELSQFDFIIPLQKPFSRGTDKTLIYPAVGEYFHFSAIWSMQHNGFLI/X | ||||
Interactor | WBInteraction000503464 | ||||
WBInteraction000503465 | |||||
WBInteraction000503466 | |||||
WBInteraction000503467 | |||||
WBInteraction000503468 | |||||
WBInteraction000503469 | |||||
WBInteraction000503470 | |||||
Isolation | Mutagen | EMS | Person_evidence | WBPerson616 | |
Genetics | Interpolated_map_position | I | -18.9835 | ||
Description | Phenotype (4) | ||||
Reference | WBPaper00035324 | ||||
Method | Deletion_allele |