WormBase Tree Display for Variation: WBVar00121867
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WBVar00121867 | Evidence | Paper_evidence | WBPaper00030778 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar00121867 | ||||
Other_name | cbs57388 | |||||
HGVSg | chrI:g.3519850C>G | |||||
Sequence_details | SMap | S_parent | Sequence | cb25.fpc3857b | ||
Flanking_sequences | tcgttttctttgctgattgatatccattctttcttccaccgccgccggat | gtttcaagcagcacatgataataagaatgagtgtcaagatgagaatcaga | ||||
Mapping_target | cb25.fpc3857b | |||||
Type_of_mutation | Substitution | C | G | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Predicted_SNP | ||||||
RFLP | Reference_strain_digest | GATC | BfuCI, BscFI, Bsp143I, BstENII, BstKTI, ChaI, DpnI, DpnII, Kzo9I, MboI, NdeII, Sau3AI | 491 393 103 13 | ||
CCNNNNNNNGG | Bsc4I, BseLI, BsiYI, BslI | 630 305 47 18 | ||||
Polymorphic_strain_digest | GATC | BfuCI, BscFI, Bsp143I, BstENII, BstKTI, ChaI, DpnI, DpnII, Kzo9I, MboI, NdeII, Sau3AI | 393 13 | |||
CCNNNNNNNGG | Bsc4I, BseLI, BsiYI, BslI | 432 305 198 47 18 | ||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis briggsae | ||||
Strain | WBStrain00041077 | |||||
Laboratory | CP | |||||
Person | WBPerson3706 | |||||
WBPerson227 | ||||||
WBPerson225 | ||||||
Status | Live | |||||
Affects | Gene | WBGene00035290 | ||||
WBGene00035291 | ||||||
Transcript | CBG14916.1 | VEP_consequence | 3_prime_UTR_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | CBG14916.1:c.*1633C>G | |||||
cDNA_position | 2200 | |||||
Exon_number | 10/20 | |||||
CBG14916.2 | VEP_consequence | 3_prime_UTR_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | CBG14916.2:c.*1633C>G | |||||
cDNA_position | 2200 | |||||
Exon_number | 10/19 | |||||
CBG14916.3 | VEP_consequence | 3_prime_UTR_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | CBG14916.3:c.*1396C>G | |||||
cDNA_position | 1963 | |||||
Exon_number | 9/19 | |||||
CBG14916.4 | VEP_consequence | 3_prime_UTR_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | CBG14916.4:c.*1396C>G | |||||
cDNA_position | 1963 | |||||
Exon_number | 9/18 | |||||
CBG14917a.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | |||||
HGVSc | CBG14917a.1:c.3326G>C | |||||
HGVSp | CBP45241.1:p.Arg1109Pro | |||||
cDNA_position | 3326 | |||||
CDS_position | 3326 | |||||
Protein_position | 1109 | |||||
Exon_number | 10/14 | |||||
Codon_change | cGa/cCa | |||||
Amino_acid_change | R/P | |||||
CBG14917b.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | |||||
HGVSc | CBG14917b.1:c.3413G>C | |||||
HGVSp | CBP42473.1:p.Arg1138Pro | |||||
cDNA_position | 3413 | |||||
CDS_position | 3413 | |||||
Protein_position | 1138 | |||||
Exon_number | 11/15 | |||||
Codon_change | cGa/cCa | |||||
Amino_acid_change | R/P | |||||
CBG14917c.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | |||||
HGVSc | CBG14917c.1:c.3413G>C | |||||
HGVSp | CBP41214.1:p.Arg1138Pro | |||||
cDNA_position | 3413 | |||||
CDS_position | 3413 | |||||
Protein_position | 1138 | |||||
Exon_number | 11/16 | |||||
Codon_change | cGa/cCa | |||||
Amino_acid_change | R/P | |||||
CBG14917d.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | |||||
HGVSc | CBG14917d.1:c.3326G>C | |||||
HGVSp | CBP38503.1:p.Arg1109Pro | |||||
cDNA_position | 3326 | |||||
CDS_position | 3326 | |||||
Protein_position | 1109 | |||||
Exon_number | 10/15 | |||||
Codon_change | cGa/cCa | |||||
Amino_acid_change | R/P | |||||
Reference | WBPaper00030778 | |||||
Remark | Predicted by: ssaha-SNP v2.0 | |||||
This SNP was observed in 1 sequencing read(s) | ||||||
Method | SNP |