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WormBase Tree Display for Variation: WBVar01703540

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Name Class

WBVar01703540NamePublic_nameWBVar01703540
Other_namecewivar00400895
R12H7.1a.2:c.957A>T
CE51729:p.Gly255=
R12H7.1a.1:c.957A>T
CE28246:p.Gly319=
R12H7.1b.1:c.765A>T
HGVSgCHROMOSOME_X:g.13214974A>T
Sequence_detailsSMapS_parentSequenceR12H7
Flanking_sequencesTTTTCACTGCAGGCAGCTCAACTTTGTTGGAAGTATCTGACTGGAATCGAGGGATATAAA
Mapping_targetR12H7
Source_location225CHROMOSOME_X1321490513214905From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00008273From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006749
TranscriptR12H7.1a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScR12H7.1a.2:c.957A>T
HGVSpCE28246:p.Gly319=
cDNA_position1083
CDS_position957
Protein_position319
Exon_number9/11
Codon_changeggA/ggT
Amino_acid_changeG
R12H7.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScR12H7.1a.1:c.957A>T
HGVSpCE28246:p.Gly319=
cDNA_position999
CDS_position957
Protein_position319
Exon_number8/10
Codon_changeggA/ggT
Amino_acid_changeG
R12H7.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScR12H7.1b.1:c.765A>T
HGVSpCE51729:p.Gly255=
cDNA_position765
CDS_position765
Protein_position255
Exon_number5/6
Codon_changeggA/ggT
Amino_acid_changeG
MethodWGS_Flibotte