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WormBase Tree Display for Variation: WBVar00014681

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Name Class

WBVar00014681EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar00014681
Other_namepas14533
haw1754
cewivar00068098
Y48G8AL.1a.2:c.1239T>G
CE49524:p.Ser37=
CE49497:p.Ser82=
Y48G8AL.1b.1:c.246T>G
CE29116:p.Ser413=
Y48G8AL.1a.1:c.1239T>G
Y48G8AL.1c.1:c.111T>G
HGVSgCHROMOSOME_I:g.1234526T>G
Sequence_detailsSMapS_parentSequenceY48G8AL
Flanking_sequencesaaattgaatgagataatctaccaatatatatgcaataaagggcaataatttcaaaaaagtcaacttcggatagattcgacacacagaaatatgggaaaaattcgagattttagctgaattcagtgaaattttgaaccaccataaaaaatttttttgaaaaccttttgagcagttttcattacttttgagcaaagttttggtcgatacgttcaaaatcgtctgaacctagttagtcctcctttaaatatatataacttcaatattcagactaatcgaatcagtattctcatcactggcctcatgaatatgtcattcttgtataaagatgaacgtcgttataatgtcggattctgttttgaacggtctcatggaattgatatggatcaagttatggaggcatttatgctttttgatgaatatccaatgaaacggcagtatatggaattggtaatacatgaaacaattggaaaaatgctttttttttggtcgataattttctaaatttttaataagtttttttttgcggaaaaaattaatttgaaattagtttttttgcgaatggtctcgtaaaattaaggtacctaaatttcacatctgttc
Mapping_targetY48G8AL
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (32)
LaboratoryAX
RW
PersonWBPerson6900
WBPerson1562
AnalysisWGS_Pasadena_Quinlan
WGS_De_Bono
Million_mutation_project_reanalysis
WGS_Hawaiian_Waterston
HistoryAcquires_mergeWBVar00148504
WBVar01277416
StatusLive
AffectsGeneWBGene00021685
TranscriptY48G8AL.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScY48G8AL.1b.1:c.246T>G
HGVSpCE49497:p.Ser82=
cDNA_position246
CDS_position246
Protein_position82
Exon_number3/13
Codon_changetcT/tcG
Amino_acid_changeS
Y48G8AL.1c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScY48G8AL.1c.1:c.111T>G
HGVSpCE49524:p.Ser37=
cDNA_position111
CDS_position111
Protein_position37
Exon_number2/12
Codon_changetcT/tcG
Amino_acid_changeS
Y48G8AL.1a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScY48G8AL.1a.2:c.1239T>G
HGVSpCE29116:p.Ser413=
cDNA_position1242
CDS_position1239
Protein_position413
Exon_number9/20
Codon_changetcT/tcG
Amino_acid_changeS
Y48G8AL.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScY48G8AL.1a.1:c.1239T>G
HGVSpCE29116:p.Ser413=
cDNA_position1249
CDS_position1239
Protein_position413
Exon_number9/20
Codon_changetcT/tcG
Amino_acid_changeS
ReferenceWBPaper00037807
MethodWGS_Pasadena_Quinlan