WormBase Tree Display for Variation: WBVar00142933
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WBVar00142933 | Evidence | Paper_evidence | WBPaper00002646 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | e49 | |||||
Other_name (9) | |||||||
HGVSg | CHROMOSOME_IV:g.7202315G>A | ||||||
Sequence_details | SMap | S_parent | Sequence | R13A1 | |||
Flanking_sequences | ctaccatctgaagagcatagacattgtaat | cgaagtcaaaaattgatcgttagttttttt | |||||
Mapping_target | R13A1 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00002646 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin (4) | |||||||
Affects | Gene | WBGene00006748 | |||||
Transcript | R13A1.4d.1 (12) | ||||||
R13A1.4c.1 (12) | |||||||
R13A1.4a.1 (12) | |||||||
R13A1.4b.1 (12) | |||||||
Genetics | Interpolated_map_position | IV | 3.29389 | ||||
Mapping_data | In_2_point | 107 | |||||
In_multi_point (24) | |||||||
In_pos_neg_data | 2737 | ||||||
3701 | |||||||
5318 | |||||||
Description | Phenotype (3) | ||||||
Reference (12) | |||||||
Remark | n49 is a typo of e49 | Paper_evidence | WBPaper00043983 | ||||
Method | Substitution_allele |