WormBase Tree Display for Variation: WBVar00248991
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WBVar00248991 | Name | Public_name | sy435 | |||
---|---|---|---|---|---|---|
Other_name | CE08038:p.Ala722Val | |||||
C09E10.2a.1:c.2165C>T | ||||||
C09E10.2d.1:c.1703C>T | ||||||
C09E10.2e.1:c.2072C>T | ||||||
CE38269:p.Ala568Val | ||||||
CE38268:p.Ala566Val | ||||||
C09E10.2b.1:c.2171C>T | ||||||
CE38270:p.Ala691Val | ||||||
CE08039:p.Ala724Val | ||||||
C09E10.2c.1:c.1697C>T | ||||||
HGVSg | CHROMOSOME_X:g.986218G>A | |||||
Sequence_details (5) | ||||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Laboratory | PS | |||||
Status | Live | |||||
Affects | Gene | WBGene00000958 | ||||
Transcript | C09E10.2d.1 (12) | |||||
C09E10.2c.1 (12) | ||||||
C09E10.2a.1 (12) | ||||||
C09E10.2e.1 (12) | ||||||
C09E10.2b.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | |||||
SIFT | 0 | deleterious | ||||
PolyPhen | 0.998 | probably_damaging | ||||
HGVSc | C09E10.2b.1:c.2171C>T | |||||
HGVSp | CE08039:p.Ala724Val | |||||
cDNA_position | 2314 | |||||
CDS_position | 2171 | |||||
Protein_position | 724 | |||||
Exon_number | 12/18 | |||||
Codon_change | gCa/gTa | |||||
Amino_acid_change | A/V | |||||
Genetics | Interpolated_map_position | X | -18.8717 | |||
Method | Substitution_allele |