WormBase Tree Display for Variation: WBVar00144643
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WBVar00144643 | Evidence | Paper_evidence | WBPaper00044385 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | e2219 | |||||
Other_name | F38A5.7.1:c.361G>A | ||||||
CE10038:p.Gly121Arg | |||||||
HGVSg | CHROMOSOME_IV:g.6602126G>A | ||||||
Sequence_details | SMap | S_parent | Sequence | F15B10 | |||
Flanking_sequences | tgggagtgtaccacttacatggagtgcatc | gatttgcgattgcaaagaagttggaggaca | |||||
Mapping_target | F15B10 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00044385 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin (3) | |||||||
Affects | Gene | WBGene00018164 | |||||
Transcript | F38A5.7.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | ||||||
SIFT | 0 | deleterious | |||||
PolyPhen | 1 | probably_damaging | |||||
HGVSc | F38A5.7.1:c.361G>A | ||||||
HGVSp | CE10038:p.Gly121Arg | ||||||
cDNA_position | 393 | ||||||
CDS_position | 361 | ||||||
Protein_position | 121 | ||||||
Exon_number | 3/4 | ||||||
Codon_change | Gga/Aga | ||||||
Amino_acid_change | G/R | ||||||
Genetics | Interpolated_map_position | IV | 3.21306 | ||||
Reference | WBPaper00044385 | ||||||
Method | Substitution_allele |