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WormBase Tree Display for Variation: WBVar00603581

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Name Class

WBVar00603581EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar00603581
Other_name (15)
HGVSgCHROMOSOME_X:g.10824185G>A
Sequence_detailsSMapS_parentSequenceF31B12
Flanking_sequencesTCGTATTTTGTACACTAACAACAATTTTTGATCTGAAAATCTAAAATTGAATTCACTTACTCATCATGTTGAACAATTGACTCGACTTCCTACTCGATCACCCATTCCAACGTACACTAAAACTCTAGCAGCATGGTACTTTACAAAAGT
Mapping_targetF31B12
Type_of_mutationSubstitutionga
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00027649From_analysisWGS_Stein
WBStrain00027653From_analysisWGS_Andersen
WBStrain00027656From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Stein
WGS_Andersen
DB_infoDatabasedbSNP_ssssss477720786
HistoryAcquires_mergeWBVar01470955
StatusLive
AffectsGeneWBGene00004036
TranscriptF31B12.1j.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF31B12.1j.1:c.2245C>T
HGVSpCE53177:p.Leu749=
cDNA_position2245
CDS_position2245
Protein_position749
Exon_number19/64
Codon_changeCtg/Ttg
Amino_acid_changeL
F31B12.1g.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF31B12.1g.1:c.2245C>T
HGVSpCE53231:p.Leu749=
cDNA_position2245
CDS_position2245
Protein_position749
Exon_number19/64
Codon_changeCtg/Ttg
Amino_acid_changeL
F31B12.1d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF31B12.1d.1:c.2416C>T
HGVSpCE53487:p.Leu806=
cDNA_position2416
CDS_position2416
Protein_position806
Exon_number20/65
Codon_changeCtg/Ttg
Amino_acid_changeL
F31B12.1h.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF31B12.1h.1:c.2245C>T
HGVSpCE53334:p.Leu749=
cDNA_position2245
CDS_position2245
Protein_position749
Exon_number19/64
Codon_changeCtg/Ttg
Amino_acid_changeL
F31B12.1l.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF31B12.1l.1:c.2245C>T
HGVSpCE53383:p.Leu749=
cDNA_position2245
CDS_position2245
Protein_position749
Exon_number19/64
Codon_changeCtg/Ttg
Amino_acid_changeL
F31B12.1i.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF31B12.1i.1:c.2416C>T
HGVSpCE53434:p.Leu806=
cDNA_position2416
CDS_position2416
Protein_position806
Exon_number20/65
Codon_changeCtg/Ttg
Amino_acid_changeL
F31B12.1k.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF31B12.1k.1:c.2416C>T
HGVSpCE53272:p.Leu806=
cDNA_position2416
CDS_position2416
Protein_position806
Exon_number20/65
Codon_changeCtg/Ttg
Amino_acid_changeL
ReferenceWBPaper00040707
Remarkvalidatation rate is over 97%
MethodWGS_Stein