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WormBase Tree Display for Variation: WBVar02137445

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Name Class

WBVar02137445EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh4793
Other_nameF58G11.2a.1:c.2418G>A
F58G11.2b.1:c.2400G>A
CE44827:p.Gln806=
CE46130:p.Gln800=
CE46471:p.Gln787=
F58G11.2c.1:c.2361G>A
HGVSgCHROMOSOME_V:g.13668384G>A
Sequence_detailsSMapS_parentSequenceF58G11
Flanking_sequencesTTTCAGGCCGTGGAAAGAGTGGAACTAGCGGTTTTGGTCACGAGGTGGATACGGAGGAAGAGGTGGAGGCTTCGGTGGCA
Mapping_targetCHROMOSOME_V
Source_location200CHROMOSOME_V1366836613668366
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023661
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00010280
TranscriptF58G11.2c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF58G11.2c.1:c.2361G>A
HGVSpCE46471:p.Gln787=
cDNA_position2371
CDS_position2361
Protein_position787
Exon_number7/9
Codon_changecaG/caA
Amino_acid_changeQ
F58G11.2a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF58G11.2a.1:c.2418G>A
HGVSpCE44827:p.Gln806=
cDNA_position2430
CDS_position2418
Protein_position806
Exon_number7/9
Codon_changecaG/caA
Amino_acid_changeQ
F58G11.2b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF58G11.2b.1:c.2400G>A
HGVSpCE46130:p.Gln800=
cDNA_position2404
CDS_position2400
Protein_position800
Exon_number7/9
Codon_changecaG/caA
Amino_acid_changeQ
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose