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WormBase Tree Display for Variation: WBVar00246278

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Name Class

WBVar00246278EvidencePaper_evidenceWBPaper00004703
NamePublic_nameWBVar00246278
Other_namesnp_T16G12[1]
T16G12.3.3:c.*923C>T
T16G12.3.1:c.*923C>T
T16G12.12.1:c.-14+136C>T
T16G12.3.5:c.*787+136C>T
T16G12.3.4:c.*787+136C>T
T16G12.3.2:c.*787+136C>T
HGVSgCHROMOSOME_III:g.10053998C>T
Sequence_detailsSMapS_parentSequenceT16G12
Flanking_sequencesgtgttgtcacttgggctccgcagagcccgtccgtccaactttgcggatataggcgcttggtcaggttcacccacgaacccacaatcaccatccgcatgagtcgctcactctctgttccattcgttcactcagaaacattccattctttaattaattaaatattattatttgaattaccgccatttgcgtatttcctaatgcaagtgcgcccccccccccg
Mapping_targetT16G12
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
RFLP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Wicks
AnalysisSNP_Wicks
StatusLive
AffectsGeneWBGene00269433
WBGene00011804
TranscriptT16G12.3.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT16G12.3.2:c.*787+136C>T
Intron_number8/8
T16G12.12.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT16G12.12.1:c.-14+136C>T
Intron_number1/5
T16G12.3.3VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScT16G12.3.3:c.*923C>T
cDNA_position1533
Exon_number7/7
T16G12.3.5VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT16G12.3.5:c.*787+136C>T
Intron_number7/7
T16G12.3.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScT16G12.3.1:c.*923C>T
cDNA_position1847
Exon_number8/8
T16G12.3.4VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT16G12.3.4:c.*787+136C>T
Intron_number7/7
ReferenceWBPaper00004703
RemarkPredicted SNP: Psnp=0.6951 VarS=CT
Enzymes. Bristol-specific: [BsmFI,BspLU11III,BstOZ616I]. CB4856-specific [none].
[20040130 db] this Locus was previously named snp_T16G12.1
[20040130 db] this Allele was previously named snp_T16G12.1
[20090224 db] original Wicks name : T16G12:11524..12399@196 Psnp=0.6951 VarS=CT
[20090224 db] original Wicks id : vd51d08.s1@140,t,32
[20090224 db] Snip-SNP
MethodSNP_Wicks