WormBase Tree Display for Variation: WBVar00142818
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WBVar00142818 | Evidence | Paper_evidence | WBPaper00005054 | |||
---|---|---|---|---|---|---|
Name | Public_name | dh8 | ||||
Other_name | T13C5.1c.1:c.467G>A | |||||
CE27206:p.Gly192Glu | ||||||
T13C5.1b.1:c.530G>A | ||||||
CE30451:p.Gly177Glu | ||||||
CE53632:p.Gly156Glu | ||||||
T13C5.1a.1:c.575G>A | ||||||
HGVSg | CHROMOSOME_X:g.6199167G>A | |||||
Sequence_details | SMap | S_parent | Sequence | T13C5 | ||
Flanking_sequences | ttttcactggagatcgtctgaacggcgatg | agttattcttgccatgcgtcagaagtggaa | ||||
Mapping_target | T13C5 | |||||
Type_of_mutation | Substitution | g | a | |||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin (3) | ||||||
Affects | Gene | WBGene00000905 | ||||
Transcript | T13C5.1c.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | |||||
SIFT | 0 | deleterious | ||||
PolyPhen | 1 | probably_damaging | ||||
HGVSc | T13C5.1c.1:c.467G>A | |||||
HGVSp | CE53632:p.Gly156Glu | |||||
cDNA_position | 467 | |||||
CDS_position | 467 | |||||
Protein_position | 156 | |||||
Exon_number | 3/10 | |||||
Codon_change | gGa/gAa | |||||
Amino_acid_change | G/E | |||||
T13C5.1b.1 (12) | ||||||
T13C5.1a.1 (12) | ||||||
Genetics | Interpolated_map_position | X | -3.46908 | |||
Reference | WBPaper00005054 | |||||
Method | Substitution_allele |