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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs174603          
refSNP ID: rs174603
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:79/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
Ancestral Allele:Not available
Clinical Association:unknown
HGVS Names
NM_004265.2:c.882+1204G>A
NT_033903.7:g.6932001G>A
Links

SNP Details are organized in the following sections:
Submission Fasta Resource GeneView Map Diversity Validation

  Submitter records for this RefSNP Cluster back to top
The submission ss2067500 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs174603 during BLAST analysis for the current build.

NCBI
Assay ID
Handle|Submitter IDValidation
Status
ss to rs
Orientation
/Strand
Alleles5' Near Seq 30 bp3' Near Seq 30 bpEntry
Date
Update
Date
Build
Added
Molecule
Type
Freq
Warning
Ancestral
Allele
Success
Rate
ss232441KWOK|OVLP-000621-97565rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt06/30/0010/10/0379Genomic94 %
ss829443SC_JCM|AC004228.2_87850rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt07/27/0010/10/0385Genomicunknown
ss1271976KWOK|OVLP-000804-332314rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt09/02/0010/10/0386Genomic94 %
ss2067500KWOK|OVLP-000925-466288rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt10/07/0010/10/0387Genomic94 %
ss2067569KWOK|OVLP-000925-469444fwd/BC/Taaaatacaaaaattagccaggcatggtggcggcgcctgtactcccagctactcaggaggt10/07/0010/10/0387Genomic94 %
ss12128187WI_SSAHASNP|chr11.NT_033903.5_6727473rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt07/04/0310/10/03116Genomicunknown
ss16162777SC_SNP|NT_033903.6_6799248rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt11/18/0311/22/03120Genomicunknown
ss16526634CSHL-HAPMAP|CSHL-HuAA-200402.chr11.NT_033903.6_6799248rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt02/17/0403/04/04120Genomicunknown
ss17423751CSHL-HAPMAP|CSHL-HuCC-200402.chr11.NT_033903.6_6799248rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt02/19/0403/04/04120Genomicunknown
ss19910875CSHL-HAPMAP|CSHL-HuFF-200402.chr11.NT_033903.6_6799248rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt02/21/0403/04/04120Genomicunknown
ss40000514ABI|hCV26712874rev/TA/Gacctcctgagtagctgggagtacaggcgccgccaccatgcctggctaatttttgtatttt07/16/0507/16/05126Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs174603|allelePos=1300|totalLen=2209|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=126
 TGCCATCCCC TTTTAGGAAC ACAGGGTGAT TTCTTTTCCT GTTTAATACT TTGTTCCTTA
 GGGAACAAGC ACAGTCAAAA ACAAACAAAA AAAAGAAGTT gctcactgca agctccgcct
 cccgggttca agcaattctc ctgcctcagc ctcctgagta gctgggacta caggtgcaca
 ccacgatgcc aggctaattt tttgtatttt tagtagagac ggggtttcac catgctggcc
 aggctggtct cgaactcctg acctcatgat ctgcccgcct cggcctctca aagtgctggg
 ataacaagca tgagtgactg cgcccggcAA TAGGCCACTT ATGAGTTAGA ACGGGATTGG
 ATGCTAGAGG CAAGGAGAGG GTGTAACATG TATAAGGAGG GAAAAAACAT AATGGTGCTA
 GTCTCTAACT TGAGCCACTG GGTGGATGAT GGAGCCATTC ATTAACATGG AGACCATCAG
 GATTAGGTTG TGGGAGAAGA GGAGAGGACT TACATTGAAT ATGTTGGATT TGAAATGGCT
 GGGACACCTC CAAATGGAGT TAGATTGGAT ATATGGGTCC AAGAATTGGA GATAAAATTT
 GACTTGGCTG CTCTTAAATT CACAGTCAGG GTGAAAAGGA CAACTTCAGT TAGCAAGCGA
 TAAAACAGTA ATCAACAggc cgggcgcggt ggctcacgcc tgtaatccca gcactttggg
 aggctgaggt gggcagatca cctcaggttg ggagtttgag accagcctga ccaacatggt
 gaaaccctgt ctctgctaaa aatacaaaat tagctgggca tggtggcgca tgcctgtaat
 cccagctact tcggaggctg aggcaggaga attactcgaa cccaggaggc agaggtttcg
 gtgagccgag atcacgccat tgtactccag cctgggcaac aagagcgaaa ctccacctca
 aaaacaaaca aacaaacaaa aaaCAGTAAT CAATAAACAA GTCCACATTT GGTTAAGAGA
 GGAAAAACTT CCCCATGGCT ATTGGTTGGA GCATGAGGGA CAAATAGACT GCTGAGAAAG
 ACTGGATTTT AAGCAAGCAT TTCAGAAAGT GACAATTTAG TCTTTGATAA TTTTCAGATA
 AACAATTTAT CTgccgggtg cagtggctca cgcctgtaat cccagcactt tgggaggcca
 aggcgggtgg atcacgagtc aagagttcga gaccaccctg gccaacatgg tgaaacccca
 tcactactaa aaatacaaaa attagccagg catggtggc
 Y
 ggcgcctgta ctcccagcta ctcaggaggt tgaggcagga gaatcgcttg aacccaggag
 gcggaggttg cagtgagccg agatcgcacc actgcactcc agcctgggcg acagagcgaa
 acaccatctc aaaaaaaaaa Gatgacgtaa ttacaatggg ccctaatgca atatgaccaa
 tgtccctatt ttaaaaaaaa ggaaaAATTT TCAAGAATCC ACTTTTGGTG AAGaaaaaaa
 gaaaattaaa aaataggcca ggcgtggtgg ctcatgcctg taatctcagc actttgtgag
 gctgaggcgg gcagatcact tgaggccagg agttcgagac cagcctcgcc aacatggaaa
 aaccccatct ctactaaaaa tacaaaaatt agctgggcat ggtggccggt gcctgtaatc
 ccaggtactt gggaggctga gtcacaagaa ttgcttgcac ccaggaggta gaggttgcag
 tgagtcgaga tcacaccact gcactccagc ctatgtgact ctgtctcaat aaataaacaa
 ataaacaaaa taattttttt aaaGAGGGAT ATTTGGACAC AGATACAGAT ACAAATATGC
 AGAGAGATGA TGTACCGAGA GGGAGGACGA AAGCCATCAA CCAGCCGATG AGAGGCCCAG
 AACAGAGCCT TCCAgagccc taaggaatcc accctgctaa cacctcagtt ttggacttcc
 ggtctccaga accgggagaa aacacatcgc tgctgcttat gccactcagt tcgtggtgct
 ttgtcataCG GTCTTCGCAA ACGACCACAC CTGTCATCTC AGCCAACGCC CAGCTGCTCC
 AACTTCAAAC CAGGGTGTGG GGCAACCCAG TTCATGGGAC TCAGGGCCCA CAGGGAGCGG
 GGAAGGGAG

  GeneView back to top
GeneView via analysis of contig annotation: FADS2 fatty acid desaturase 2
View variations for gene:
Include clinically associated: in gene region cSNP has frequency double hit
Group
Label
Contig->mRNAGene Model (contig mRNA transcript) Color Legend
referenceNT_033903->NM_004265
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_033903->NM_004265->NP_0042566932001forwardintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs174603 maps exactly once on NCBI human chromosome 11
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
11NW_001838024.172620257954418minusGalt_assembly_8HuRefHuRefview1299
11NW_925106.1730962658961550minusGalt_assembly_1CeleraCeleraview1299
11NT_033903.7693200161382782minusGref_assemblyreferencereferenceview1299

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_033903 AC004770.1 AF139813.1 AP000591 AP002380
dbSNP Blast Analysis
GenBank HTGS Finished:
AF139813.1 AP002380.3 AP006260.2

  Population Diversity back to top
There is no frequency data.

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterwith2hit
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .