Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar02140700

expand all nodes | collapse all nodes | view schema

Name Class

WBVar02140700EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh14068
Other_nameCE47951:p.Ala71=
F39D8.3b.1:c.213C>T
F39D8.3a.2:c.90C>T
CE34014:p.Ala30=
F39D8.3a.1:c.90C>T
HGVSgCHROMOSOME_X:g.15422614C>T
Sequence_detailsSMapS_parentSequenceF39D8
Flanking_sequencesAACACTCTCGCCAAAAACGATCGGTGTCTCCAATTTCCGCTCGTTGCCTAATCGGTGATCCAATGTTCCGAGTTGCATCC
Mapping_targetCHROMOSOME_X
Source_location200CHROMOSOME_X1542253515422535
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023886
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00009561
TranscriptF39D8.3a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF39D8.3a.2:c.90C>T
HGVSpCE34014:p.Ala30=
cDNA_position121
CDS_position90
Protein_position30
Exon_number2/10
Codon_changegcC/gcT
Amino_acid_changeA
F39D8.3a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF39D8.3a.1:c.90C>T
HGVSpCE34014:p.Ala30=
cDNA_position313
CDS_position90
Protein_position30
Exon_number3/11
Codon_changegcC/gcT
Amino_acid_changeA
F39D8.3b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF39D8.3b.1:c.213C>T
HGVSpCE47951:p.Ala71=
cDNA_position213
CDS_position213
Protein_position71
Exon_number2/9
Codon_changegcC/gcT
Amino_acid_changeA
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose