WormBase Tree Display for Variation: WBVar00109178
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WBVar00109178 | Evidence | Paper_evidence | WBPaper00030778 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar00109178 | ||||
Other_name | cbs44699 | |||||
HGVSg | chrII:g.5099372A>G | |||||
Sequence_details | SMap | S_parent | Sequence | cb25.fpc0072a | ||
Flanking_sequences | taatttacttctttacctttctgaatacttgaattcagccccattgttgt | aggctttcacgggggtcatattaaattaactatatcaaatctaccgtaaa | ||||
Mapping_target | cb25.fpc0072a | |||||
Type_of_mutation | Substitution | A | G | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Predicted_SNP | ||||||
RFLP | Reference_strain_digest | RAATTY | AcsI, ApoI, XapI | 371 210 131 99 76 73 20 20 | ||
GAATTC | EcoRI, FunII | 520 480 | ||||
CAC | HindI | 247 240 143 116 73 58 54 40 15 11 3 | ||||
TCNNGA | Hpy178III, Hpy188III | 675 153 151 21 | ||||
TCNGA | Hpy188I | 462 376 95 67 | ||||
GTNAC | MaeIII | 955 45 | ||||
TTAA | MseI, Tru1I, Tru9I | 254 190 189 177 107 78 5 | ||||
CAYNNNNRTG | MslI, SmiMI | 1000 | ||||
GTSAC | NmuCI, Tsp45I | 1000 | ||||
AATT | Sse9I, TasI, Tsp509I, TspEI | 146 132 114 99 64 63 58 48 43 40 34 33 30 20 20 18 17 12 9 | ||||
Polymorphic_strain_digest | RAATTY | AcsI, ApoI, XapI | 371 210 149 131 99 20 20 | |||
GAATTC | EcoRI, FunII | 1000 | ||||
CAC | HindI | 247 240 143 107 73 54 40 30 19 15 11 9 9 3 | ||||
TCNNGA | Hpy178III, Hpy188III | 606 153 151 69 21 | ||||
TCNGA | Hpy188I | 529 376 95 | ||||
GTNAC | MaeIII | 486 469 45 | ||||
TTAA | MseI, Tru1I, Tru9I | 254 190 189 177 78 66 41 5 | ||||
CAYNNNNRTG | MslI, SmiMI | 505 495 | ||||
GTSAC | NmuCI, Tsp45I | 514 486 | ||||
AATT | Sse9I, TasI, Tsp509I, TspEI | 146 132 114 99 64 63 58 58 48 43 34 33 30 20 20 17 12 9 | ||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis briggsae | ||||
Strain | WBStrain00041077 | |||||
Laboratory | CP | |||||
Person | WBPerson3706 | |||||
WBPerson227 | ||||||
WBPerson225 | ||||||
Status | Live | |||||
Affects | Gene | WBGene00027010 | ||||
Transcript | CBG04307.1 | VEP_consequence | 3_prime_UTR_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | CBG04307.1:c.*1202A>G | |||||
cDNA_position | 3918 | |||||
Exon_number | 21/21 | |||||
CBG04307.2 | VEP_consequence | 3_prime_UTR_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | CBG04307.2:c.*1246A>G | |||||
cDNA_position | 3536 | |||||
Exon_number | 19/19 | |||||
CBG04307.3 | VEP_consequence | 3_prime_UTR_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | CBG04307.3:c.*1212A>G | |||||
cDNA_position | 3502 | |||||
Exon_number | 20/20 | |||||
Reference | WBPaper00030778 | |||||
Remark | Predicted by: ssaha-SNP v2.0 | |||||
This SNP was observed in 1 sequencing read(s) | ||||||
Method | SNP |