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: WBVar00038261

expand all nodes | collapse all nodes | view schema

Name Class

WBVar00038261NamePublic_nameWBVar00038261
Other_namepas19249
cewivar00080049
F56D12.1b.1:c.*547C>T
CE29047:p.Leu506=
CE40074:p.Leu366=
F56D12.1d.1:c.1098C>T
F56D12.1a.2:c.1518C>T
F56D12.1a.1:c.1518C>T
HGVSgCHROMOSOME_II:g.1306559G>A
Sequence_detailsSMapS_parentSequenceY57G7A
Flanking_sequencesttatgcgatcacgggggaaaaaaaattaaaattcagtggtaaagcaataattgttgacctaatcaaaaagaaaactatattctcaatatgagaaaaatcggaaatgaaaagaaaaaaacaacataattattccattgatggatatttccagtcagtcaatgacaccgacgtctccttaatcgtcagcggcgaggtccatcggagcccatagtgggggccaccggccttatcattggttccggacaatctggagcctccgaatggctgctggccgacgattgatccagttgatttgtcgttaggtacatgttgccgacggcgtcgcggagaacatcgcgagctctgagaaaaaaaaacactttgttgaaaaacgtttttaacacaaaaattcgcctcaaaaatctcgaaaaatcgatcgaaatccaacaaaaattccaataaaaaataccgtagccctttaaagggacacacactttcactgttgggtctcgccacgctcaggaacatcttactgtcgctttcaaattttttgtttgttgttatcgcttttttttttcgatttttgccagtttttctagcttttcatttgatttgtgacga
Mapping_targetY57G7A
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00004604From_analysisWGS_Pasadena_Quinlan
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000112
TranscriptF56D12.1b.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScF56D12.1b.1:c.*547C>T
cDNA_position2088
Exon_number8/8
F56D12.1a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.2:c.1518C>T
HGVSpCE29047:p.Leu506=
cDNA_position1617
CDS_position1518
Protein_position506
Exon_number9/10
Codon_changectC/ctT
Amino_acid_changeL
F56D12.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.1:c.1518C>T
HGVSpCE29047:p.Leu506=
cDNA_position1521
CDS_position1518
Protein_position506
Exon_number8/9
Codon_changectC/ctT
Amino_acid_changeL
F56D12.1d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1d.1:c.1098C>T
HGVSpCE40074:p.Leu366=
cDNA_position1098
CDS_position1098
Protein_position366
Exon_number4/4
Codon_changectC/ctT
Amino_acid_changeL
MethodWGS_Pasadena_Quinlan