WormBase Tree Display for Variation: WBVar00603581
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WBVar00603581 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar00603581 | ||||
Other_name (15) | ||||||
HGVSg | CHROMOSOME_X:g.10824185G>A | |||||
Sequence_details | SMap | S_parent | Sequence | F31B12 | ||
Flanking_sequences | TCGTATTTTGTACACTAACAACAATTTTTGATCTGAAAATCTAAAATTGAATTCACTTACTCATCATGTTGAACA | ATTGACTCGACTTCCTACTCGATCACCCATTCCAACGTACACTAAAACTCTAGCAGCATGGTACTTTACAAAAGT | ||||
Mapping_target | F31B12 | |||||
Type_of_mutation | Substitution | g | a | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00027649 | From_analysis | WGS_Stein | |||
WBStrain00027653 | From_analysis | WGS_Andersen | ||||
WBStrain00027656 | From_analysis | WGS_Andersen | ||||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | WGS_Stein | |||||
WGS_Andersen | ||||||
DB_info | Database | dbSNP_ss | ss | ss477720786 | ||
History | Acquires_merge | WBVar01470955 | ||||
Status | Live | |||||
Affects | Gene | WBGene00004036 | ||||
Transcript | F31B12.1j.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | |||||
HGVSc | F31B12.1j.1:c.2245C>T | |||||
HGVSp | CE53177:p.Leu749= | |||||
cDNA_position | 2245 | |||||
CDS_position | 2245 | |||||
Protein_position | 749 | |||||
Exon_number | 19/64 | |||||
Codon_change | Ctg/Ttg | |||||
Amino_acid_change | L | |||||
F31B12.1g.1 | VEP_consequence | synonymous_variant | ||||
VEP_impact | LOW | |||||
HGVSc | F31B12.1g.1:c.2245C>T | |||||
HGVSp | CE53231:p.Leu749= | |||||
cDNA_position | 2245 | |||||
CDS_position | 2245 | |||||
Protein_position | 749 | |||||
Exon_number | 19/64 | |||||
Codon_change | Ctg/Ttg | |||||
Amino_acid_change | L | |||||
F31B12.1d.1 | VEP_consequence | synonymous_variant | ||||
VEP_impact | LOW | |||||
HGVSc | F31B12.1d.1:c.2416C>T | |||||
HGVSp | CE53487:p.Leu806= | |||||
cDNA_position | 2416 | |||||
CDS_position | 2416 | |||||
Protein_position | 806 | |||||
Exon_number | 20/65 | |||||
Codon_change | Ctg/Ttg | |||||
Amino_acid_change | L | |||||
F31B12.1h.1 | VEP_consequence | synonymous_variant | ||||
VEP_impact | LOW | |||||
HGVSc | F31B12.1h.1:c.2245C>T | |||||
HGVSp | CE53334:p.Leu749= | |||||
cDNA_position | 2245 | |||||
CDS_position | 2245 | |||||
Protein_position | 749 | |||||
Exon_number | 19/64 | |||||
Codon_change | Ctg/Ttg | |||||
Amino_acid_change | L | |||||
F31B12.1l.1 | VEP_consequence | synonymous_variant | ||||
VEP_impact | LOW | |||||
HGVSc | F31B12.1l.1:c.2245C>T | |||||
HGVSp | CE53383:p.Leu749= | |||||
cDNA_position | 2245 | |||||
CDS_position | 2245 | |||||
Protein_position | 749 | |||||
Exon_number | 19/64 | |||||
Codon_change | Ctg/Ttg | |||||
Amino_acid_change | L | |||||
F31B12.1i.1 | VEP_consequence | synonymous_variant | ||||
VEP_impact | LOW | |||||
HGVSc | F31B12.1i.1:c.2416C>T | |||||
HGVSp | CE53434:p.Leu806= | |||||
cDNA_position | 2416 | |||||
CDS_position | 2416 | |||||
Protein_position | 806 | |||||
Exon_number | 20/65 | |||||
Codon_change | Ctg/Ttg | |||||
Amino_acid_change | L | |||||
F31B12.1k.1 | VEP_consequence | synonymous_variant | ||||
VEP_impact | LOW | |||||
HGVSc | F31B12.1k.1:c.2416C>T | |||||
HGVSp | CE53272:p.Leu806= | |||||
cDNA_position | 2416 | |||||
CDS_position | 2416 | |||||
Protein_position | 806 | |||||
Exon_number | 20/65 | |||||
Codon_change | Ctg/Ttg | |||||
Amino_acid_change | L | |||||
Reference | WBPaper00040707 | |||||
Remark | validatation rate is over 97% | |||||
Method | WGS_Stein |