Preferred Name

observed_variation
ID

observed_variation
Full Id

http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#observed_variation
comment

It is the variation (of nucleotides or of residues) observed between the 2 patients (reference sequence and the alternative sequence - if it's possible to talk about a "reference") when a genomic variation is described. Ex: A>C, CT>A, Ser>Thr, etc.
disjointWith

sequence_position

database

variant

sequence

Map From

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