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Click on the image below to view the connections between Entrez SNP and other databases. |
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dbSNP is now incorporated into NCBI's Entrez system and can be queried using
the same approach as the other Entrez databases such as PubMed and GenBank.
The original database with additional information and search options are available
here.
- Enter one or more search terms.
- Available search fields are listed below
- Use Limits to restrict your search by search field, chromosome, and other criteria.
Update: |
August 14, 2002 |
Add contig position tag [CTPOS] |
Below are search examples and available search fields.
Either the search fields or qualifiers (aliases)
can be use for querying SNP (i.e. 103[CBID]
is same as 103[Create
Build ID]. Data type marked with an asterisk (*) indicates range
searching is available.
Allele |
[ALLELE],[VARIATION],
[VARI] |
IUPAC |
Observed allele(s)
Example: N[ALLELE]
|
Chromosome |
[CHR] |
Textnum |
Mapped chromosome number
Available values [1-22,W-Z, and Un (unknown)]
Example: 2[CHR]
or X[CHR] |
Base Position |
[CHRPOS],[BPOS] |
Integer* |
Mapped chromosome position; use in conjunction with chromosome
field [CHR]
Example: 7[CHR]
AND 88556398:88580839[CHRPOS] |
Create Build ID |
[CREATE_BUILD],[CBID] |
Integer* |
SNP create build ID
Example: 103[CBID]
|
Publication Date |
[CREATEDATE],[CDAT],[PDAT], [PUBDATE] |
Date* |
SNP create/publication date
Use the format YYYY/MM/DD; month and day are optional.
Example: 2002/01[CDATE] |
Function Class |
[FXN_CLASS], [FUNC] |
Text |
Function Class:
locus region |
intron |
coding nonsynon |
mrna utr |
coding synon |
reference |
exception |
splice site |
Example: "coding
synon"[FUNC] |
Gene Name |
[GENE], [GENE_SYMBOL] |
Textnum |
Locus link symbol
Example: LPL[GENE]
|
Protein Description |
[PDSC] |
Text |
Protein description
Example: "liver
expressed"[PDSC] |
Gene Description |
[GDSC] |
Text |
Gene description
Example: "kinase"[Gene
Description] |
GO Terms |
[GO] |
Text |
Gene Ontology (GO) terms
Example: "receptor"[GO
term] |
Genotype |
[GENOTYPE], [GTYPE] |
Boolean |
Genotype
Example: true[GTYPE] |
Heterozygosity |
[HET] |
Integer* |
Heterozygosity(%)
Example: 5[HET]
|
Local SNP ID |
[LOC_SNP_ID] |
Textnum |
Submitter local SNP ID
Example: "TSC0227737"[LOC_SNP_ID] |
LocusLink ID |
[LOCUS_ID],[LID] |
Integer |
LocusLink ID number
Example: 4023[LID]
|
Map Weight |
[WEIGHT],[MPWT],[HIT] |
Integer* |
SNP map weight info - the number of times a SNP map to
the genome contig (range 1-10)
1 = |
hit genome once, annotated on NT_ contigs |
2 = |
hit genome twice, annotated on NT_ contigs with warning |
3 = |
hit genome 3-9 times, not annotated |
10 = |
hit 10+ times on genome, not annotated |
Example: 1[WEIGHT] |
Method Class |
[METHOD_CLASS], [METHOD], [MCLS] |
Text |
Assay method used
to identify SNP:
computed |
rflp |
dhplc |
sequence |
hybridize |
sscp |
other |
unknown |
Example: "sequence"[METHOD] |
Accession |
[ACC] |
Textnum |
Search by nucleotide or protein accession
Example: AC000120[ACC]
|
Contig Position |
[CTPOS] |
|
Mapped contig position; use in conjunction with contig accession field
[ACC]
1000000:2000000[CTPOS]
AND NT_034874[ACC] |
Reference SNP ID |
[RS] |
Integer* |
dbSNP assigned reference SNP ID (RS)
Example: rs709932[RS]
|
Submitter SNP ID |
[SS] |
Integer* |
dbSNP assigned submitter SNP ID (SS)
Example: ss1487247[SS]
|
Population Class |
[POP_CLASS],[POP],[PCLS] |
Text |
Population
Classification based on geographic location:
central asia |
north america |
central south africa |
north/east africa & middle
east |
central south america |
pacific |
east asia |
unknown |
europe |
west africa |
multi national |
|
Example: "europe"[POP] |
SNP Class |
[SNP_CLASS], [SCLS] |
Text |
SNP Class/type:
het |
mnp |
in del |
named |
microsat |
no variation |
mixed |
snp |
Example: "snp"[SNP_CLASS]
|
Submitter Handle |
[HANDLE] |
Text |
Submitter handle
Example: "LEE"[HANDLE]
|
Success Rate |
[SUCCESS_RATE], [SRATE] |
Integer* |
Success rate(%)
Example: 95[SRATE] |
Organism |
[ORGN],[TAX_ID] |
Text |
Organism name
or Taxonomy ID number; use the prefix 'txid' before the Taxonomy ID number
Example: "human"[ORGN] ,
"mouse"[ORGN],
or "txid9606"[ORGN] |
Update Build ID |
[UPD_BUILD],[UBID] |
Integer* |
SNP update build ID
Example: 102[UBID]
|
Modification Date |
[UDATE], [UDAT], [MODDATE] |
Date* |
SNP modification/update date
Use the format YYYY/MM/DD; month and day are optional.
Example: 2002/01
[UDATE] |
Validation |
[VALIDATION] |
Text |
Validation status:
by cluster |
by submitter |
by frequency |
no info |
Example: "by
cluster"[VALIDATION]
|
central asia |
Samples from Russia and satellite Republics, Nations bordering Indian Ocean between East Asia and Persian Gulf regions. |
central south africa |
Nations south of Equator, Madagascar & neighboring Island Nations. |
central south america |
Samples from Mainland Central and South America, Island Nations of western Atlantic, Gulf of Mexico and Eastern Pacific. |
east asia |
Samples from Eastern and South Eastern Mainland Asia, Northern Pacific Island Nations. |
europe |
Samples from Europe north and west of Caucasus Mountains, Scandinavia, Atlantic Islands. |
multi national |
samples that were designed to maximize measures of heterogeneity or sample human diversity in a global fashion. Examples OEFNER|GLOBAL and CEPH repository. |
north america |
All samples north of Tropic of Cancer. This would include defined samples of U.S. Caucasians, African Americans and Hispanics and NCBI|NIHPDR. |
north/east africa & middle east |
samples collected from North Africa (including Sahara desert), East Africa (south to Equator), Levant, Persian Gulf. |
pacific |
Samples from Australia, New Zealand, Central and Southern Pacific Islands, Southeast Asian Peninsular/Island Nations. |
unknown |
Samples with unknown geographic provenience that are not global in nature. |
west africa |
Sub-Saharan Nations bordering Atlantic north of Congo River, and Central/Southern Atlantic Island Nations. |
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|
computed |
variation was mined from sequence alignment with software |
dhplc |
Denaturing High Pressure Liquid Chromatography used to detect SNP |
hybridize |
hybridization method (e.g. chip) was used to assay for variation |
other |
other method used to detect variation |
rflp |
variation in enzyme restriction site used to detect variation |
sequence |
samples were sequenced and resulting alignment used to define variation |
sscp |
single stranded conformational polymorphism used to detect variation |
unknown |
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|
het |
variation has unknown sequence composition, but is observed to be heterozygous |
in del |
insertion deletion polymorophism, deletions represented by '-' in allele string |
microsat |
microsatellite / simple sequence repeat |
mixed |
|
mnp |
multiple nucleotide polymorphism (all alleles same length where length>1) |
named |
allele sequences defined by name tag instead of raw sequence, e.g. (Alu)/- |
no variation |
submission reports invariant region in surveyed sequence |
snp |
true single nucleotide polymorphism |
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IUPAC code
|
Meaning |
A |
A |
C |
C |
G |
G |
T |
T |
M |
A or C |
R |
A or G |
W |
A or T |
S |
C or G |
Y |
C or T |
K |
G or T |
V |
A or C or G |
H |
A or C or T |
D |
A or G or T |
B |
C or G or T |
N |
G or A or T or C |
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Homo sapiens |
Arabidopsis thaliana |
Caenorhabditis elegans |
Ficedula albicollis |
Ficedula hypoleuca |
Gallus gallus |
Mus musculus |
Pan troglodytes |
Plasmodium falciparum |
Rattus norvegicus |
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