WormBase Tree Display for Variation: WBVar00302762
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WBVar00302762 | Evidence | Paper_evidence | WBPaper00036201 | ||
---|---|---|---|---|---|
Name | Public_name | otn5941 | |||
Other_name | OH6087_694820 | ||||
CE14964:p.Ile578= | |||||
Y57G11C.22a.1:c.101-2447A>T | |||||
Y57G11C.20.1:c.1734A>T | |||||
HGVSg | CHROMOSOME_IV:g.14845095A>T | ||||
Sequence_details | SMap | S_parent | Sequence | Y57G11C | |
Flanking_sequences | TTCGGTAACGTTAGCACAATCTATCTTTATTGTGATATTGTAGACCCTAT | ATCGTGGGAGATTCTAAAAATTCGCTACTGTCTGTAATTCCCTGTAAAGG | |||
Mapping_target | Y57G11C | ||||
Type_of_mutation | Substitution | A | T | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00029489 | ||||
Laboratory | OTN | ||||
Analysis | WGS_Hobert | ||||
Status | Live | ||||
Affects | Gene | WBGene00013315 | |||
WBGene00013317 | |||||
Transcript | Y57G11C.20.1 | VEP_consequence | synonymous_variant | ||
VEP_impact | LOW | ||||
HGVSc | Y57G11C.20.1:c.1734A>T | ||||
HGVSp | CE14964:p.Ile578= | ||||
cDNA_position | 1734 | ||||
CDS_position | 1734 | ||||
Protein_position | 578 | ||||
Exon_number | 1/1 | ||||
Codon_change | atA/atT | ||||
Amino_acid_change | I | ||||
Y57G11C.22a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y57G11C.22a.1:c.101-2447A>T | ||||
Intron_number | 2/7 | ||||
Genetics | Map | IV | |||
Reference | WBPaper00036201 | ||||
Method | WGS_Hobert |