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WormBase Tree Display for Variation: WBVar00000331

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Name Class

WBVar00000331EvidencePaper_evidenceWBPaper00005629
NamePublic_nameay39
Other_nameT28F12.2b.1:c.1552C>T
CE50189:p.Gln477Ter
CE31074:p.Gln102Ter
CE21219:p.Gln555Ter
T28F12.2h.1:c.1429C>T
T28F12.2d.5:c.304C>T
CE33585:p.Gln551Ter
T28F12.2d.2:c.304C>T
CE21220:p.Gln518Ter
T28F12.2e.1:c.1540C>T
T28F12.2c.1:c.430C>T
T28F12.2d.3:c.304C>T
T28F12.2f.1:c.1651C>T
T28F12.2d.8:c.304C>T
CE37795:p.Gln481Ter
CE31073:p.Gln144Ter
T28F12.2d.1:c.304C>T
T28F12.2d.6:c.304C>T
T28F12.2g.1:c.1441C>T
T28F12.2d.4:c.304C>T
T28F12.2d.9:c.304C>T
T28F12.2d.7:c.304C>T
T28F12.2c.2:c.430C>T
CE33584:p.Gln514Ter
T28F12.2d.10:c.304C>T
T28F12.2a.1:c.1663C>T
HGVSgCHROMOSOME_V:g.4510859C>T
Sequence_detailsSMapS_parentSequenceT28F12
Flanking_sequencesgtggctccaacagtagatgctctttctcaaaatgggttgatctctcagcaccacacgaat
Mapping_targetT28F12
Type_of_mutationSubstitutionctPaper_evidenceWBPaper00005629
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryNH
StatusLive
AffectsGeneWBGene00006796
TranscriptT28F12.2d.7VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.7:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position1089
CDS_position304
Protein_position102
Exon_number7/8
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2a.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2a.1:c.1663C>T
HGVSpCE21219:p.Gln555Ter
cDNA_position1667
CDS_position1663
Protein_position555
Exon_number11/12
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2b.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2b.1:c.1552C>T
HGVSpCE21220:p.Gln518Ter
cDNA_position2018
CDS_position1552
Protein_position518
Exon_number11/12
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2d.2VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.2:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position1675
CDS_position304
Protein_position102
Exon_number11/12
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2d.3VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.3:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position2027
CDS_position304
Protein_position102
Exon_number11/12
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2d.8VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.8:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position831
CDS_position304
Protein_position102
Exon_number6/7
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2c.2VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2c.2:c.430C>T
HGVSpCE31073:p.Gln144Ter
cDNA_position2172
CDS_position430
Protein_position144
Exon_number10/11
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2d.9VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.9:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position1172
CDS_position304
Protein_position102
Exon_number5/6
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2d.10VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.10:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position3013
CDS_position304
Protein_position102
Exon_number3/4
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2h.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2h.1:c.1429C>T
HGVSpCE50189:p.Gln477Ter
cDNA_position1429
CDS_position1429
Protein_position477
Exon_number9/9
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2d.4VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.4:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position1860
CDS_position304
Protein_position102
Exon_number11/12
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2e.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2e.1:c.1540C>T
HGVSpCE33584:p.Gln514Ter
cDNA_position1540
CDS_position1540
Protein_position514
Exon_number10/10
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2d.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.1:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position1655
CDS_position304
Protein_position102
Exon_number11/12
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2c.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2c.1:c.430C>T
HGVSpCE31073:p.Gln144Ter
cDNA_position2357
CDS_position430
Protein_position144
Exon_number10/11
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2d.5VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.5:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position1547
CDS_position304
Protein_position102
Exon_number10/11
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2d.6VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2d.6:c.304C>T
HGVSpCE31074:p.Gln102Ter
cDNA_position1211
CDS_position304
Protein_position102
Exon_number8/9
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2g.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2g.1:c.1441C>T
HGVSpCE37795:p.Gln481Ter
cDNA_position1441
CDS_position1441
Protein_position481
Exon_number9/9
Codon_changeCaa/Taa
Amino_acid_changeQ/*
T28F12.2f.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScT28F12.2f.1:c.1651C>T
HGVSpCE33585:p.Gln551Ter
cDNA_position1655
CDS_position1651
Protein_position551
Exon_number11/11
Codon_changeCaa/Taa
Amino_acid_changeQ/*
GeneticsInterpolated_map_positionV-5.16203
ReferenceWBPaper00005629
MethodSubstitution_allele