WormBase Tree Display for Variation: WBVar02137882
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WBVar02137882 | Evidence | Paper_evidence | WBPaper00045317 | |||
---|---|---|---|---|---|---|
Name | Public_name | h14995 | ||||
Other_name | Y32B12C.5:n.1275+1382G>A | |||||
CE19067:p.Phe178= | ||||||
Y32B12C.1.1:c.534C>T | ||||||
HGVSg | CHROMOSOME_V:g.16607274C>T | |||||
Sequence_details | SMap | S_parent | Sequence | Y32B12C | ||
Flanking_sequences | ACGAGCAACTGTGGGACTTTGACAATATTCCTGATGGATT | CAGCCAATGCTGGAACTGCACCATTTAAAAAAAGACCAAG | ||||
Mapping_target | CHROMOSOME_V | |||||
Source_location | 200 | CHROMOSOME_V | 16607247 | 16607247 | ||
Type_of_mutation | Substitution | C | T | |||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00023767 | |||||
Laboratory | KR | |||||
Analysis | WGS_Rose | |||||
Status | Live | |||||
Affects | Gene | WBGene00012525 | ||||
WBGene00194769 | ||||||
Transcript | Y32B12C.1.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | |||||
HGVSc | Y32B12C.1.1:c.534C>T | |||||
HGVSp | CE19067:p.Phe178= | |||||
cDNA_position | 540 | |||||
CDS_position | 534 | |||||
Protein_position | 178 | |||||
Exon_number | 4/6 | |||||
Codon_change | ttC/ttT | |||||
Amino_acid_change | F | |||||
Pseudogene | Y32B12C.5 | VEP_consequence | intron_variant,non_coding_transcript_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | Y32B12C.5:n.1275+1382G>A | |||||
Intron_number | 3/3 | |||||
Reference | WBPaper00040589 | |||||
WBPaper00000975 | ||||||
WBPaper00003985 | ||||||
WBPaper00000699 | ||||||
WBPaper00045317 | ||||||
Method | WGS_Rose |