WormBase Tree Display for Variation: WBVar02125009
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WBVar02125009 | Evidence | Paper_evidence | WBPaper00044031 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | my24 | |||||
Other_name | F11A6.1a.2:c.1319C>T | ||||||
CE17653:p.Pro440Leu | |||||||
F11A6.1a.1:c.1319C>T | |||||||
HGVSg | CHROMOSOME_I:g.11679199C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | F11A6 | |||
Flanking_sequences | atatgcacacggggaccagtgcaagtgctc | gttggctgctggaattgttgctcttgctcta | |||||
Mapping_target | F11A6 | ||||||
Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00044031 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | PT | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00002232 | |||||
Transcript | F11A6.1a.1 (12) | ||||||
F11A6.1a.2 | VEP_consequence | missense_variant | |||||
VEP_impact | MODERATE | ||||||
SIFT | 0 | deleterious | |||||
PolyPhen | 1 | probably_damaging | |||||
HGVSc | F11A6.1a.2:c.1319C>T | ||||||
HGVSp | CE17653:p.Pro440Leu | ||||||
cDNA_position | 1423 | ||||||
CDS_position | 1319 | ||||||
Protein_position | 440 | ||||||
Exon_number | 5/9 | ||||||
Codon_change | cCg/cTg | ||||||
Amino_acid_change | P/L | ||||||
Genetics | Interpolated_map_position | I | 9.5394 | ||||
Reference | WBPaper00044031 | ||||||
Method | Substitution_allele |