WormBase Tree Display for Variation: WBVar00248996
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WBVar00248996 | Name | Public_name | sy454 | ||
---|---|---|---|---|---|
Other_name | C09E10.2d.1:c.1858-1G>A | ||||
C09E10.2e.1:c.2227-1G>A | |||||
C09E10.2b.1:c.2326-1G>A | |||||
C09E10.2c.1:c.1852-1G>A | |||||
C09E10.2a.1:c.2320-1G>A | |||||
HGVSg | CHROMOSOME_X:g.985974C>T | ||||
Sequence_details (5) | |||||
Variation_type | Allele | ||||
Origin (3) | |||||
Affects | Gene | WBGene00000958 | |||
Transcript | C09E10.2d.1 | VEP_consequence | splice_acceptor_variant | ||
VEP_impact | HIGH | ||||
HGVSc | C09E10.2d.1:c.1858-1G>A | ||||
Intron_number | 10/13 | ||||
C09E10.2c.1 | VEP_consequence | splice_acceptor_variant | |||
VEP_impact | HIGH | ||||
HGVSc | C09E10.2c.1:c.1852-1G>A | ||||
Intron_number | 10/13 | ||||
C09E10.2a.1 | VEP_consequence | splice_acceptor_variant | |||
VEP_impact | HIGH | ||||
HGVSc | C09E10.2a.1:c.2320-1G>A | ||||
Intron_number | 13/17 | ||||
C09E10.2e.1 | VEP_consequence | splice_acceptor_variant | |||
VEP_impact | HIGH | ||||
HGVSc | C09E10.2e.1:c.2227-1G>A | ||||
Intron_number | 11/14 | ||||
C09E10.2b.1 | VEP_consequence | splice_acceptor_variant | |||
VEP_impact | HIGH | ||||
HGVSc | C09E10.2b.1:c.2326-1G>A | ||||
Intron_number | 13/17 | ||||
Genetics | Interpolated_map_position | X | -18.8717 | ||
Method | Substitution_allele |