<variant>
cannot be filled in by submitters:       
required when defining a new element:       
at least one required when defining a new element:       
only one allowed, required when defining a new element:       
details ...

This type describes a variant. A variant must be reported on the same DNA strand as the reference sequence this experiment is on.

This information is used for submissions to dbSNP.

Attributes
pharmgkbId

A unique identifier assigned by the PharmGKB (the PharmGKB Accession Id). This attribute is used to refer to data that is already in the PharmGKB and is only supplied when editing or adding to such data. See the FAQ for details.

localId

A unique identifier for this element assigned by the submitter. The only rule it must follow is that no two XML elements can be assigned the same localId within a single XML document. See the FAQ for details.

Subelements
note

A note.

submitter

This element's submitter.

position

The position on the reference sequence where this variant is found.

allele

The allele found on a chromosome.

The allele sequence must be composed of A's, G's, C's, T's, and -'s (to denote a deletion). For repeats, the repeated bases should be enclosed within parentheses followed by the number of times the sequence is repeated (e.g. (AT)6). If the polymorphism spans multiple bases and is not an insert, then the bases should be enclosed within square brackets (e.g. [ATC]). See the FAQ for details.

xref

A cross-reference to a resource with more information on this variant.

Validation Rules

Content validation performed on this element: