Ss
Defined in file docsum.asn
C++ class: CSs
Ss ::= SEQUENCE {
attlist SET {
ssId INTEGER, --dbSNP accession number for submission
handle VisibleString, --Tag for the submitting laboratory
batchId INTEGER, --dbSNP number for batch submission
locSnpId VisibleString OPTIONAL, --submission (ss#) submitter ID
--SubSNP classification by type of
-- variation
subSnpClass ENUMERATED {
snp (1),
in-del (2),
heterozygous (3),
microsatellite (4),
named-locus (5),
no-variation (6),
mixed (7),
multinucleotide-polymorphism (8)
} OPTIONAL,
--orientation of refsnp cluster members to refsnp cluster
-- sequence
orient ENUMERATED {
forward (1),
reverse (2)
} OPTIONAL,
--strand is defined as TOP/BOTTOM by nature of flanking
-- nucleotide sequence
strand ENUMERATED {
top (1),
bottom (2)
} OPTIONAL,
molType ENUMERATED {
genomic (1),
cDNA (2),
mito (3),
chloro (4),
unknown (5)
} OPTIONAL, --moltype from Batch table
--dbSNP build number when ss# was added to a refSNP (rs#)
-- cluster
buildId INTEGER OPTIONAL,
--class of method used to assay for the
-- variation
methodClass ENUMERATED {
dHPLC (1),
hybridize (2),
computed (3),
sSCP (4),
other (5),
unknown (6),
rFLP (7),
sequence (8)
} OPTIONAL,
--subsnp has been experimentally validated by
-- submitter
validated ENUMERATED {
by-submitter (1),
by-frequency (2),
by-cluster (3)
} OPTIONAL,
--append loc-snp-id to this base URL to construct a pointer to
-- submitter data.
linkoutUrl VisibleString OPTIONAL,
ssAlias VisibleString OPTIONAL,
--
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alleleOrigin INTEGER OPTIONAL,
--
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clinicalSignificance VisibleString OPTIONAL
},
sequence SEQUENCE {
--5' sequence that flanks the
-- variation
seq5 VisibleString OPTIONAL,
--list of all nucleotide alleles observed in
-- ss-list members, correcting for reverse complementation of
-- memebers reported in reverse orientation
observed VisibleString,
--3' sequence that flanks the
-- variation
seq3 VisibleString OPTIONAL
}
}