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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs151667          
refSNP ID: rs151667
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:A/G
Ancestral Allele:G
Clinical Association:unknown
HGVS Names
NM_022726.2:c.101-7452T>C
NT_007299.12:g.18463721A>G
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 ss1730968 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs151667 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
ss308519KWOK|OVLP-000621-361966rev/BC/Tttcgtatctacctatcctgttcattgccaggcagctccctaacccaggtttccatcatct06/30/0010/10/0379Genomic97 %
ss309420KWOK|OVLP-000621-366571fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa06/30/0010/10/0379Genomic97 %
ss437387KWOK|OVLP-000621-344117fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa06/30/0010/10/0392Genomic99 %
ss440473KWOK|OVLP-000621-350926fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa06/30/0010/10/0392Genomic99 %
ss622345SC_JCM|AC011851.3_151723fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa07/12/0010/10/0392Genomicunknown
ss1070457KWOK|OVLP-000804-9765rev/BC/Tttcgtatctacctatcctgttcattgccaggcagctccctaacccaggtttccatcatct09/02/0010/10/0392Genomic99 %
ss1071898KWOK|OVLP-000804-16141fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa09/02/0010/10/0392Genomic99 %
ss1200490KWOK|OVLP-000804-20722rev/BC/Tttcgtatctacctatcctgttcattgccaggcagctccctaacccaggtttccatcatct09/02/0010/10/0392Genomic97 %
ss1201170KWOK|OVLP-000804-27739fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa09/02/0010/10/0392Genomic97 %
ss1730459KWOK|OVLP-000925-307542fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa10/05/0010/10/0392Genomic97 %
ss1730968KWOK|OVLP-000925-321671fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa10/05/0010/10/0392Genomic97 %
ss1731371KWOK|OVLP-000925-332281rev/BC/Tttcgtatctacctatcctgttcattgccaggcagctccctaacccaggtttccatcatct10/05/0010/10/0392Genomic97 %
ss1732174KWOK|OVLP-000925-340297fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa10/05/0010/10/0392Genomic97 %
ss6484848WI_SSAHASNP|NT_007299.11_12119335fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa02/12/0310/10/03111Genomicunknown
ss22484179SSAHASNP|WGSA-200403-chr6.chr6.NT_007299.12_18463721fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa03/21/0403/21/04121Genomicunknown
ss23395642PERLEGEN|afd4596971byFreqfwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa08/10/0409/13/04123Genomicunknown
ss42759446ABI|hCV3181674fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa07/18/0507/18/05126Genomicunknown
ss84779849HGSV|Cor18517_SNV_20070510.chr6_80700269fwd/TA/Gagatgatggaaacctgggttagggagctgcctggcaatgaacaggataggtagatacgaa12/06/0712/08/07130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs151667|allelePos=917|totalLen=1656|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 GCAGACAGGG AGAAAAGTCT TTTTTCAGGG GGCAGAATTA GAAAGACCTA CAAAAGTTCC
 CTTAGTACAA TGACAAGATA TAAGCAAATG AGAATATCTG AATACCCTGA GAGAACTGAA
 TGTATAAGCA GCCCAGAAGC AAGAAATAAA ACAATCTGGA AACTAAGCAG ACATGATGAA
 GAGGATATAT ACAAAGGAAG AGGGCAGGAA ATGACTGTGA TGATCCCCTA GGAGGTCTTA
 CAAACTACAC TGAGGATGCT GGAATTTATC ATGTAGATAA TGAAGAGATA tttgattgtt
 tttgtttgtt tgtttgtttg tttgtttgtt ttgggactgg gtctggctct gttgcccaga
 ctagaatgca gtggcatgat ctcagctcac tgcagcctcc acctccaggg cttaagcgat
 tttcgtgcct cagccaccca agtagcttgg actacaggtg catgccacaa cacccagcta
 atttttgtgt tttttgtaga gacgaggatt cgccatgttg ctcaggctgg ccctgaaccc
 ctgagctcaa gcaacccacc tacctcagcc tcccaaagtg ctgggattac agtcatgagc
 caccacaccc agccAGTTTT GGCTTTCAAA AGATCATGGT AGAGGCAGTG GGGTGTGGAC
 TGAGGGGAAG GGGATATGTC AAGAGGCAGG AAAACCAACT GCATcagtgg ttctcaatac
 ttgtctacca ctagactacc catgtaagaa tcatgtgctt gctaaaatta tagattccca
 ggtcctactg aatcaaaatc tctgcgggtg ggactggaca ctatgatctg agctccccca
 ggtgattctg acaggcaggc agacttggag accactAGGA CATAagagat gatggaaacc
 tgggttaggg agctgc
 R
 ctggcaatga acaggatagg tagatacgaa ggtttcgtgg gtaaaatcta cagactccac
 gactgttgtg gatgtgagag aagagagtca aagaaaagtt caggattact cccagatttc
 tggtctatct ggcaacacag acagtgaagt catgatccat aacagagtaa aggaagagga
 gcagatctgg gagaaactga tcaggtgaat gttgaacatc tcgcatctga gctacttttg
 ggacagctag gtggaggcgt ccagtagcct ctggagctgc agaggaactg ccagggctgt
 ggacacaCAG AGGGGTCACT GACAATGACA ATCACACCAG AGTTTGAGGT CACAAGGGAA
 GGAGCATGTA CAGTGAGAGA ATAACATGAA AAAGGAATGA CTCTGAGGAC AGTTGAAGAT
 GAGTGGGTGA AATGGCAGCA AATAAGCCAG AGAGGCAGGA AAAGAGAAAA CCATGTCACA
 AAGACCGAGA AATTTCCAAA AGGAAAGGGT GCAGAACAGA ATCTATAGCT GGAAAACCAA
 ctgttcttcc tttttctttt tttaatgagg aaatagttac ttcatagggt taagatgtga
 taactaaatg aaccaaagta tgcgaagGTT CCTAGCACAC ATGGATACCA CGACGTCATG
 CATTCCCTTC TGCTGCAGCC TATTCTCTCC CAAATTTACA TCTTCACAAA GTATGTCTCA
 TGTCAGAGAT AATCTGAGC

  GeneView back to top
GeneView via analysis of contig annotation: ELOVL4 elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4
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_007299->NM_022726
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_007299->NM_022726->NP_07356318463721reverseintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs151667 maps exactly once on NCBI human chromosome 6
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
6NW_001838987.11004461377866411plusAalt_assembly_8HuRefHuRefview916
6NT_007299.121846372180700269plusAref_assemblyreferencereferenceview916
6NW_923184.11313013581061531plusGalt_assembly_1CeleraCeleraview916

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_007299 AC048371 AL132875.12 AL133475 AL133475.14 AL159162.5
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AL133475.14 AL159162.7

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/G
G/G
HWPA
G
ss23395642AFD_EUR_PANELEuropean 44IG 0.727 0.227 0.045 0.527 0.841 0.159
AFD_AFR_PANELAfrican American 44IG 0.227 0.455 0.318 0.752 0.455 0.545
AFD_CHN_PANELAsian 46IG 0.739 0.261 0.479 0.870 0.130

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.400+/-0.200715000

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqwith2hit
DoubleHit found by:  BCM_SSAHASNPNCBI
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .