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WormBase Tree Display for Variation: WBVar01516101

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Name Class

WBVar01516101NamePublic_nameWBVar01516101
Other_namecewivar00039874
C11D2.6c.1:c.1242T>A
C11D2.6o.1:c.1440T>A
C11D2.6n.1:c.1440T>A
CE48950:p.Leu414=
CE49437:p.Leu474=
C11D2.6g.1:c.1422T>A
CE49155:p.Leu462=
C11D2.6e.1:c.1422T>A
C11D2.6k.1:c.1386T>A
CE48791:p.Leu474=
CE49351:p.Leu480=
CE49195:p.Leu480=
CE49459:p.Leu462=
C11D2.6p.1:c.1440T>A
CE48978:p.Leu414=
C11D2.6a.1:c.1422T>A
C11D2.6f.1:c.1242T>A
C11D2.6m.1:c.1440T>A
CE48883:p.Leu414=
CE48736:p.Leu474=
C11D2.6i.1:c.1386T>A
C11D2.6j.1:c.1386T>A
C11D2.6h.1:c.1242T>A
CE49413:p.Leu480=
CE37196:p.Leu474=
C11D2.6b.1:c.1242T>A
C11D2.6d.1:c.1422T>A
CE49219:p.Leu462=
CE49180:p.Leu414=
CE49197:p.Leu462=
C11D2.6l.1:c.1386T>A
CE49262:p.Leu480=
HGVSgCHROMOSOME_IV:g.6168124A>T
Sequence_detailsSMapS_parentSequenceC11D2
Flanking_sequencesAAGAATCTTGATGATACATTCAACATTGAAAGTATTGTGAATCCAACTTCGAAAAGATAA
Mapping_targetC11D2
Source_location225CHROMOSOME_IV61681136168113From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000032From_analysisMillion_mutation_project_reanalysis
WBStrain00022868From_analysisMillion_mutation_project_reanalysis
WBStrain00022899From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006809
TranscriptC11D2.6b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6b.1:c.1242T>A
HGVSpCE48883:p.Leu414=
cDNA_position1242
CDS_position1242
Protein_position414
Exon_number8/27
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6i.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6i.1:c.1386T>A
HGVSpCE49155:p.Leu462=
cDNA_position1386
CDS_position1386
Protein_position462
Exon_number9/29
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6a.1:c.1422T>A
HGVSpCE48736:p.Leu474=
cDNA_position1525
CDS_position1422
Protein_position474
Exon_number10/30
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6l.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6l.1:c.1386T>A
HGVSpCE49197:p.Leu462=
cDNA_position1386
CDS_position1386
Protein_position462
Exon_number9/28
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6e.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6e.1:c.1422T>A
HGVSpCE48791:p.Leu474=
cDNA_position1422
CDS_position1422
Protein_position474
Exon_number9/28
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6g.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6g.1:c.1422T>A
HGVSpCE49437:p.Leu474=
cDNA_position1422
CDS_position1422
Protein_position474
Exon_number9/28
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6m.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6m.1:c.1440T>A
HGVSpCE49195:p.Leu480=
cDNA_position1440
CDS_position1440
Protein_position480
Exon_number10/30
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6k.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6k.1:c.1386T>A
HGVSpCE49459:p.Leu462=
cDNA_position1386
CDS_position1386
Protein_position462
Exon_number9/28
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6o.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6o.1:c.1440T>A
HGVSpCE49351:p.Leu480=
cDNA_position1440
CDS_position1440
Protein_position480
Exon_number10/29
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6p.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6p.1:c.1440T>A
HGVSpCE49413:p.Leu480=
cDNA_position1440
CDS_position1440
Protein_position480
Exon_number10/29
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6f.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6f.1:c.1242T>A
HGVSpCE48950:p.Leu414=
cDNA_position1242
CDS_position1242
Protein_position414
Exon_number8/26
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6d.1:c.1422T>A
HGVSpCE37196:p.Leu474=
cDNA_position1422
CDS_position1422
Protein_position474
Exon_number9/29
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6c.1:c.1242T>A
HGVSpCE48978:p.Leu414=
cDNA_position1242
CDS_position1242
Protein_position414
Exon_number8/29
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6h.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6h.1:c.1242T>A
HGVSpCE49180:p.Leu414=
cDNA_position1242
CDS_position1242
Protein_position414
Exon_number8/27
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6n.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6n.1:c.1440T>A
HGVSpCE49262:p.Leu480=
cDNA_position1440
CDS_position1440
Protein_position480
Exon_number10/28
Codon_changectT/ctA
Amino_acid_changeL
C11D2.6j.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC11D2.6j.1:c.1386T>A
HGVSpCE49219:p.Leu462=
cDNA_position1386
CDS_position1386
Protein_position462
Exon_number9/27
Codon_changectT/ctA
Amino_acid_changeL
MethodWGS_Flibotte