WormBase Tree Display for Variation: WBVar02136565
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WBVar02136565 | Evidence | Paper_evidence | WBPaper00045317 | |||
---|---|---|---|---|---|---|
Name | Public_name | h4763 | ||||
Other_name | T07H8.4f.1:c.4312+243G>A | |||||
T07H8.4h.1:c.4876+243G>A | ||||||
T07H8.4d.1:c.4843+243G>A | ||||||
T07H8.4b.1:c.4867+243G>A | ||||||
T07H8.4e.1:c.4720+243G>A | ||||||
T07H8.4a.1:c.4879+243G>A | ||||||
T07H8.4g.1:c.3670+243G>A | ||||||
T07H8.4d.2:c.4843+243G>A | ||||||
HGVSg | CHROMOSOME_V:g.6963540G>A | |||||
Sequence_details | SMap | S_parent | Sequence | T07H8 | ||
Flanking_sequences | GAAATTTAGGATGACATACTTGGATTTTGTTTAGTTTACT | CTTTGAAATGATACATATTTTCCAGAATTGTTCAACAAAA | ||||
Mapping_target | CHROMOSOME_V | |||||
Source_location | 200 | CHROMOSOME_V | 6963522 | 6963522 | ||
Type_of_mutation | Substitution | G | A | |||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00023661 | |||||
Laboratory | KR | |||||
Analysis | WGS_Rose | |||||
Status | Live | |||||
Affects | Gene | WBGene00003165 | ||||
Transcript | T07H8.4e.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | T07H8.4e.1:c.4720+243G>A | |||||
Intron_number | 22/27 | |||||
T07H8.4b.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | T07H8.4b.1:c.4867+243G>A | |||||
Intron_number | 24/25 | |||||
T07H8.4a.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | T07H8.4a.1:c.4879+243G>A | |||||
Intron_number | 25/31 | |||||
T07H8.4h.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | T07H8.4h.1:c.4876+243G>A | |||||
Intron_number | 24/29 | |||||
T07H8.4d.2 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | T07H8.4d.2:c.4843+243G>A | |||||
Intron_number | 25/30 | |||||
T07H8.4f.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | T07H8.4f.1:c.4312+243G>A | |||||
Intron_number | 24/29 | |||||
T07H8.4g.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | T07H8.4g.1:c.3670+243G>A | |||||
Intron_number | 16/21 | |||||
T07H8.4d.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | T07H8.4d.1:c.4843+243G>A | |||||
Intron_number | 25/31 | |||||
Reference | WBPaper00040589 | |||||
WBPaper00000975 | ||||||
WBPaper00003985 | ||||||
WBPaper00000699 | ||||||
WBPaper00045317 | ||||||
Method | WGS_Rose |