WormBase Tree Display for Variation: WBVar00145031
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WBVar00145031 | Evidence | Paper_evidence | WBPaper00031667 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | e2882 | |||||
Other_name | T23F2.1a.1:c.362C>T | ||||||
CE28488:p.Pro121Leu | |||||||
T23F2.1b.1:c.404C>T | |||||||
CE54583:p.Pro135Leu | |||||||
HGVSg | CHROMOSOME_X:g.5494226C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | T23F2 | |||
Flanking_sequences | actgccattttccacaacagttagtaacac | gtctcgatttttcctgtatagatggtatgc | |||||
Mapping_target | T23F2 | ||||||
Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00031667 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain | WBStrain00004682 | ||||||
Laboratory | CB | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00044623 | |||||
Transcript | T23F2.1b.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | ||||||
HGVSc | T23F2.1b.1:c.404C>T | ||||||
HGVSp | CE54583:p.Pro135Leu | ||||||
cDNA_position | 404 | ||||||
CDS_position | 404 | ||||||
Protein_position | 135 | ||||||
Exon_number | 4/9 | ||||||
Codon_change | cCg/cTg | ||||||
Amino_acid_change | P/L | ||||||
T23F2.1a.1 | VEP_consequence | missense_variant | |||||
VEP_impact | MODERATE | ||||||
SIFT | 0.05 | tolerated | |||||
PolyPhen | 1 | probably_damaging | |||||
HGVSc | T23F2.1a.1:c.362C>T | ||||||
HGVSp | CE28488:p.Pro121Leu | ||||||
cDNA_position | 362 | ||||||
CDS_position | 362 | ||||||
Protein_position | 121 | ||||||
Exon_number | 3/9 | ||||||
Codon_change | cCg/cTg | ||||||
Amino_acid_change | P/L | ||||||
Genetics | Interpolated_map_position | X | -5.24244 | ||||
Description (2) | |||||||
Reference | WBPaper00031667 | ||||||
Method | Substitution_allele |