WormBase Tree Display for Variation: WBVar00089715
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WBVar00089715 | Evidence | Paper_evidence | WBPaper00017687 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | n733 | |||||
Other_name | W01C8.6.2:c.778G>A | ||||||
CE35792:p.Gly260Arg | |||||||
W01C8.6.1:c.778G>A | |||||||
HGVSg | CHROMOSOME_X:g.5707765C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | W01C8 | |||
Flanking_sequences | ATGGGTATAGCGCTTGGAGGCCTGGCACTG | GAGTACTAGTTGGTCCTCCGTACGGTGGAT | |||||
Mapping_target | W01C8 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00017687 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | MT | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00000295 | |||||
Transcript | W01C8.6.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | ||||||
SIFT | 0 | deleterious | |||||
PolyPhen | 1 | probably_damaging | |||||
HGVSc | W01C8.6.1:c.778G>A | ||||||
HGVSp | CE35792:p.Gly260Arg | ||||||
cDNA_position | 818 | ||||||
CDS_position | 778 | ||||||
Protein_position | 260 | ||||||
Exon_number | 7/13 | ||||||
Codon_change | Gga/Aga | ||||||
Amino_acid_change | G/R | ||||||
W01C8.6.2 | VEP_consequence | missense_variant | |||||
VEP_impact | MODERATE | ||||||
SIFT | 0 | deleterious | |||||
PolyPhen | 1 | probably_damaging | |||||
HGVSc | W01C8.6.2:c.778G>A | ||||||
HGVSp | CE35792:p.Gly260Arg | ||||||
cDNA_position | 877 | ||||||
CDS_position | 778 | ||||||
Protein_position | 260 | ||||||
Exon_number | 8/14 | ||||||
Codon_change | Gga/Aga | ||||||
Amino_acid_change | G/R | ||||||
Genetics | Interpolated_map_position | X | -4.39418 | ||||
Reference | WBPaper00017687 | ||||||
Method | Substitution_allele |