WormBase Tree Display for Variation: WBVar00246278
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WBVar00246278 | Evidence | Paper_evidence | WBPaper00004703 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00246278 | |||
Other_name | snp_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 | |||||
HGVSg | CHROMOSOME_III:g.10053998C>T | ||||
Sequence_details | SMap | S_parent | Sequence | T16G12 | |
Flanking_sequences | gtgttgtcacttgggctccgcagagcccgtccgtc | caactttgcggatataggcgcttggtcaggttcacccacgaacccacaatcaccatccgcatgagtcgctcactctctgttccattcgttcactcagaaacattccattctttaattaattaaatattattatttgaattaccgccatttgcgtatttcctaatgcaagtgcgcccccccccccg | |||
Mapping_target | T16G12 | ||||
Type_of_mutation | Substitution | C | T | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
RFLP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00004602 | From_analysis | SNP_Wicks | ||
Analysis | SNP_Wicks | ||||
Status | Live | ||||
Affects | Gene | WBGene00269433 | |||
WBGene00011804 | |||||
Transcript | T16G12.3.2 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | T16G12.3.2:c.*787+136C>T | ||||
Intron_number | 8/8 | ||||
T16G12.12.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T16G12.12.1:c.-14+136C>T | ||||
Intron_number | 1/5 | ||||
T16G12.3.3 | VEP_consequence | 3_prime_UTR_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T16G12.3.3:c.*923C>T | ||||
cDNA_position | 1533 | ||||
Exon_number | 7/7 | ||||
T16G12.3.5 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T16G12.3.5:c.*787+136C>T | ||||
Intron_number | 7/7 | ||||
T16G12.3.1 | VEP_consequence | 3_prime_UTR_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T16G12.3.1:c.*923C>T | ||||
cDNA_position | 1847 | ||||
Exon_number | 8/8 | ||||
T16G12.3.4 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T16G12.3.4:c.*787+136C>T | ||||
Intron_number | 7/7 | ||||
Reference | WBPaper00004703 | ||||
Remark | Predicted 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 | |||||
Method | SNP_Wicks |