WormBase Tree Display for Variation: WBVar00320010
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WBVar00320010 | Evidence | Paper_evidence | WBPaper00037659 | ||
---|---|---|---|---|---|
Name | Public_name | snx2438 | |||
Other_name | IS657_1446 | ||||
M01E10.2a.1:c.2069C>A | |||||
CE54093:p.Ser690Tyr | |||||
M01E10.2b.1:c.1353+110C>A | |||||
HGVSg | CHROMOSOME_III:g.2041919G>T | ||||
Sequence_details | SMap | S_parent | Sequence | M01E10 | |
Flanking_sequences | CCTCGATTTTCACGATCTCGTCTACAGTATACCGGCGTGGGGTTACGGTA | AAGTGGGCGTGGTCTCGGTTACTGTAGAAGGTGGTGACGTCATTGGGGTT | |||
Mapping_target | M01E10 | ||||
Type_of_mutation | Substitution | G | T | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00022164 | ||||
Laboratory | IS | ||||
Analysis | WGS_Jarriault | ||||
Status | Live | ||||
Affects | Gene | WBGene00001063 | |||
Transcript | M01E10.2a.1 | VEP_consequence | missense_variant | ||
VEP_impact | MODERATE | ||||
HGVSc | M01E10.2a.1:c.2069C>A | ||||
HGVSp | CE54093:p.Ser690Tyr | ||||
cDNA_position | 2079 | ||||
CDS_position | 2069 | ||||
Protein_position | 690 | ||||
Exon_number | 11/22 | ||||
Codon_change | tCt/tAt | ||||
Amino_acid_change | S/Y | ||||
M01E10.2b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | M01E10.2b.1:c.1353+110C>A | ||||
Intron_number | 6/16 | ||||
Genetics | Map | III | |||
Reference | WBPaper00037659 | ||||
Method | WGS_Jarriault |