WormBase Tree Display for Variation: WBVar00144541
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WBVar00144541 | Evidence | Paper_evidence | WBPaper00001677 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | e2072 | |||||
Other_name | F02A9.6.1:c.410G>A | ||||||
CE00237:p.Gly137Glu | |||||||
HGVSg | CHROMOSOME_III:g.9094741G>A | ||||||
Sequence_details | SMap | S_parent | Sequence | F02A9 | |||
Flanking_sequences | acaacggactctgctatccattctatggtg | atttcagtgcatatgcaacaatggatatgg | |||||
Mapping_target | F02A9 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00001677 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain | WBStrain00022555 | ||||||
Laboratory | CB | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00001609 | |||||
Transcript | F02A9.6.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | ||||||
SIFT | 0.04 | deleterious | |||||
PolyPhen | 1 | probably_damaging | |||||
HGVSc | F02A9.6.1:c.410G>A | ||||||
HGVSp | CE00237:p.Gly137Glu | ||||||
cDNA_position | 482 | ||||||
CDS_position | 410 | ||||||
Protein_position | 137 | ||||||
Exon_number | 5/11 | ||||||
Codon_change | gGa/gAa | ||||||
Amino_acid_change | G/E | ||||||
Isolation | Mutagen | EMS | |||||
Genetics | Interpolated_map_position | III | 0.162813 | ||||
Description | Phenotype (12) | ||||||
Reference | WBPaper00027246 | ||||||
WBPaper00003363 | |||||||
WBPaper00001008 | |||||||
WBPaper00016588 | |||||||
WBPaper00016490 | |||||||
Method | Substitution_allele |