WormBase Tree Display for Variation: WBVar00437026
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WBVar00437026 | Name | Public_name | gk213783 | |||
---|---|---|---|---|---|---|
Other_name (18) | ||||||
HGVSg | CHROMOSOME_IV:g.11985080C>T | |||||
Sequence_details | SMap | S_parent | Sequence | ZK617 | ||
Flanking_sequences | TGTAGCAGTGAGCTCACCGGCTCCAACCGTGACAGCTGGTACCCAGTCTC | TGATGGAGTTCTCATTTCAACGAGATATCCTTCGATTGGAGCACCTCCAT | ||||
Mapping_target | ZK617 | |||||
Type_of_mutation | Substitution | C | T | |||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00038500 | |||||
Laboratory | VC | |||||
Analysis | Million_Mutation_Project | |||||
Status | Live | |||||
Affects | Gene | WBGene00006759 | ||||
Transcript | ZK617.1i.1 (11) | |||||
ZK617.1a.1 (11) | ||||||
ZK617.1g.1 (11) | ||||||
ZK617.1f.1 (11) | ||||||
ZK617.1d.1 (11) | ||||||
ZK617.1c.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | |||||
PolyPhen | 0.981 | probably_damaging | ||||
HGVSc | ZK617.1c.1:c.8899G>A | |||||
HGVSp | CE47057:p.Gly2967Arg | |||||
cDNA_position | 9160 | |||||
CDS_position | 8899 | |||||
Protein_position | 2967 | |||||
Exon_number | 22/26 | |||||
Codon_change | Gga/Aga | |||||
Amino_acid_change | G/R | |||||
ZK617.1h.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | |||||
HGVSc | ZK617.1h.1:c.10468G>A | |||||
HGVSp | CE49973:p.Gly3490Arg | |||||
cDNA_position | 10468 | |||||
CDS_position | 10468 | |||||
Protein_position | 3490 | |||||
Exon_number | 30/34 | |||||
Codon_change | Gga/Aga | |||||
Amino_acid_change | G/R | |||||
ZK617.1b.1 | VEP_consequence | missense_variant | ||||
VEP_impact | MODERATE | |||||
HGVSc | ZK617.1b.1:c.10516G>A | |||||
HGVSp | CE33018:p.Gly3506Arg | |||||
cDNA_position | 10516 | |||||
CDS_position | 10516 | |||||
Protein_position | 3506 | |||||
Exon_number | 30/34 | |||||
Codon_change | Gga/Aga | |||||
Amino_acid_change | G/R | |||||
ZK617.1e.1 (11) | ||||||
Reference | WBPaper00042537 | |||||
Method | Million_mutation |