WormBase Tree Display for Variation: WBVar00248952
expand all nodes | collapse all nodes | view schema
WBVar00248952 | Evidence | Paper_evidence | WBPaper00029156 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | sy262 | |||||
Other_name | T28F12.3b.1:c.964G>A | ||||||
CE53014:p.Gly322Arg | |||||||
CE36328:p.Gly322Arg | |||||||
T28F12.3a.1:c.964G>A | |||||||
HGVSg | CHROMOSOME_V:g.4543812C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | Y61A9LA | |||
Flanking_sequences | gagctcagcgatactcaatgtattggaatg | gaatttgggagcacggagaagcttatgaat | |||||
Mapping_target | Y61A9LA | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00029156 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | PS | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00004947 | |||||
Transcript | T28F12.3a.1 (12) | ||||||
T28F12.3b.1 | VEP_consequence | missense_variant | |||||
VEP_impact | MODERATE | ||||||
SIFT | 0.01 | deleterious | |||||
PolyPhen | 0.997 | probably_damaging | |||||
HGVSc | T28F12.3b.1:c.964G>A | ||||||
HGVSp | CE53014:p.Gly322Arg | ||||||
cDNA_position | 964 | ||||||
CDS_position | 964 | ||||||
Protein_position | 322 | ||||||
Exon_number | 6/20 | ||||||
Codon_change | Gga/Aga | ||||||
Amino_acid_change | G/R | ||||||
Isolation | Mutagen | EMS | Paper_evidence | WBPaper00029156 | |||
Genetics | Interpolated_map_position | V | -5.05797 | ||||
Description (2) | |||||||
Reference | WBPaper00029156 | ||||||
Method | Substitution_allele |