WormBase Tree Display for Variation: WBVar00000240
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WBVar00000240 | Evidence | Paper_evidence | WBPaper00005695 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | ar224 | |||||
Other_name | F02A9.6.1:c.2185G>A | ||||||
CE00237:p.Ala729Thr | |||||||
HGVSg | CHROMOSOME_III:g.9097121G>A | ||||||
Sequence_details | SMap | S_parent | Sequence | F02A9 | |||
Flanking_sequences | acagcgcaaagtgtcgttgatttgattgct | ctggacttgtgaagtctgatgtaagttatt | |||||
Mapping_target | F02A9 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00005695 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain | WBStrain00052667 | ||||||
Laboratory | GS | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00001609 | |||||
Transcript | F02A9.6.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | ||||||
SIFT | 0.01 | deleterious | |||||
PolyPhen | 0.999 | probably_damaging | |||||
HGVSc | F02A9.6.1:c.2185G>A | ||||||
HGVSp | CE00237:p.Ala729Thr | ||||||
cDNA_position | 2257 | ||||||
CDS_position | 2185 | ||||||
Protein_position | 729 | ||||||
Exon_number | 7/11 | ||||||
Codon_change | Gct/Act | ||||||
Amino_acid_change | A/T | ||||||
Genetics | Interpolated_map_position | III | 0.163857 | ||||
Reference | WBPaper00005695 | ||||||
WBPaper00061946 | |||||||
Remark | A729T, extracellular domain | ||||||
Method | Substitution_allele |