WormBase Tree Display for Variation: WBVar00143145
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WBVar00143145 | Evidence | Paper_evidence | WBPaper00004985 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | e359 | |||||
Other_name | ZC416.8a.1:c.1039G>C | ||||||
ZC416.8b.1:c.1-1285G>C | |||||||
CE17307:p.Gly347Arg | |||||||
HGVSg | CHROMOSOME_IV:g.3619060C>G | ||||||
Sequence_details | SMap | S_parent | Sequence | ZC416 | |||
Flanking_sequences | gcgattgctatggttgggttggctatggag | gaatcgcgtgttttgcaatcccctatacca | |||||
Mapping_target | ZC416 | ||||||
Type_of_mutation | Substitution | g | m | Paper_evidence | WBPaper00004985 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | CB | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00006756 | |||||
WBGene00000481 | |||||||
Transcript | ZC416.8a.1 (12) | ||||||
ZC416.8b.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | ZC416.8b.1:c.1-1285G>C | ||||||
Intron_number | 1/11 | ||||||
Genetics | Interpolated_map_position | IV | -3.11559 | ||||
Reference | WBPaper00004985 | ||||||
Remark | Manually curated Gene associations preserved as a text remark so that VEP is the canonical predictor of consequence: WBGene00006756 Missense 347 G to R Inferred_automatically map_Alleles.pl | ||||||
Method | Substitution_allele |