WormBase Tree Display for Variation: WBVar00116391
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WBVar00116391 | Evidence | Paper_evidence | WBPaper00030778 | |||
---|---|---|---|---|---|---|
WBPaper00055507 | ||||||
Name | Public_name | WBVar00116391 | ||||
Other_name | cbs51912 | |||||
cb51912 | Paper_evidence | WBPaper00055507 | ||||
HGVSg | chrII:g.4378311G>A | |||||
Sequence_details | SMap | S_parent | Sequence | cb25.fpc2441 | ||
Flanking_sequences | ccaatttcactccattcaactcgac | tcagcgatacatccaacgaagttat | ||||
Mapping_target | cb25.fpc2441 | |||||
Type_of_mutation | Substitution | G | A | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Predicted_SNP | ||||||
RFLP | Reference_strain_digest | GACGTC | AatII, ZraI | 501 499 | ||
GRCGYC | AcyI, BsaHI, BstACI, Hin1I, Hsp92I | 502 478 20 | ||||
ATGCAT | BfrBI, EcoT22I, Mph1103I, NsiI, Ppu10I, Zsp2I | 1000 | ||||
TCGA | EsaBC3I, TaqI, TthHB8I | 469 212 109 109 33 31 27 10 | ||||
CAC | HindI | 194 98 91 80 72 66 62 61 42 41 37 36 28 27 24 18 15 8 | ||||
CGWCG | Hpy99I | 500 500 | ||||
ACGT | HpyCH4IV, MaeII, TaiI, TscI | 502 215 144 139 | ||||
Polymorphic_strain_digest | GACGTC | AatII, ZraI | 1000 | |||
GRCGYC | AcyI, BsaHI, BstACI, Hin1I, Hsp92I | 980 20 | ||||
ATGCAT | BfrBI, EcoT22I, Mph1103I, NsiI, Ppu10I, Zsp2I | 582 418 | ||||
TCGA | EsaBC3I, TaqI, TthHB8I | 387 212 109 109 82 33 31 27 10 | ||||
CAC | HindI | 194 98 91 80 72 66 62 61 51 42 41 37 28 27 24 18 8 | ||||
CGWCG | Hpy99I | 535 465 | ||||
ACGT | HpyCH4IV, MaeII, TaiI, TscI | 641 215 144 | ||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis briggsae | ||||
Strain | WBStrain00041077 | |||||
Laboratory | CP | |||||
Person | WBPerson3706 | |||||
WBPerson227 | ||||||
WBPerson225 | ||||||
Status | Live | |||||
Affects | Gene | WBGene00032251 | ||||
Transcript | CBG11064c.1 | VEP_consequence | 3_prime_UTR_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | CBG11064c.1:c.*1616C>T | |||||
cDNA_position | 12277 | |||||
Exon_number | 46/46 | |||||
CBG11064g.1 | VEP_consequence | synonymous_variant | ||||
VEP_impact | LOW | |||||
HGVSc | CBG11064g.1:c.12006C>T | |||||
HGVSp | CBP43908.1:p.Asp4002%3D | |||||
cDNA_position | 12006 | |||||
CDS_position | 12006 | |||||
Protein_position | 4002 | |||||
Exon_number | 45/45 | |||||
Codon_change | gaC/gaT | |||||
Amino_acid_change | D | |||||
Reference | WBPaper00030778 | |||||
WBPaper00055507 | ||||||
Remark | Predicted by: ssaha-SNP v2.0 | |||||
This SNP was observed in 1 sequencing read(s) | ||||||
Method | SNP |