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BUILD 130
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Reference SNP(refSNP) Cluster Report: rs34898343          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:126/130
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_002612.3:c.326A>G
NP_002603.1:p.Asp109Gly
NT_007933.14:g.20457305T>C
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 ss48534216 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs34898343 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
ss48534216CANCER-GENOME|NC_000007.11_94867680fwd/BC/Tcatagagcttactctgataatgctttctggcatctgggcttttctcatggaattccacca10/20/0511/29/05126Genomicunknown
ss69022741PERLEGEN|PGP14523541byFreqfwd/BC/Tcatagagcttactctgataatgctttctggcatctgggcttttctcatggaattccacca01/30/0703/31/08127Genomicunknown
ss86257825CORNELL|hCV25921848fwd/TA/Gcatagagcttactctgataatgctttctggcatctgggcttttctcatggaattccacca01/21/0801/21/08130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs34898343|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=130
 TCATTTTCAA TGCCATATTT CTTCGCTTCT GAAAAACCAA CAAGCCAAAA CTTGTCATGT
 GTAAGAGGGT AGTGATTTAT TATTCAGAGC TGAATTCCTT TAATTTAGGT CTAAAAATAT
 CTTAGGAATC TATCTGGAAA GAACCAAAGT TTTAAACACT TATTCTAATG CATAGAGCTT
 ACTCTGATAA TGCTTTCTGG
 Y
 CATCTGGGCT TTTCTCATGG AATTCCACCA AATCCATCAG GCTCTGTATA TACCTGTAAA
 GAAACAGGTA TGCTTTAAGT TTTAAAATTA ATAGTCAGAT ACAAATGGCT GAAAATAGAA
 TAGCTTTTTC AAATAATTTG AAAAGAGAAA GTAAGCATTA TGTTCAAACT TAAAACTTTC
 CTCCAGAACA TTTGGAAAAT

  GeneView back to top

GeneView via analysis of contig annotation:  

View more variation on this gene (click to hide).
Include clinically associated: in gene region cSNP has frequency double hit
Assembly SNP to Chr Chr Chr position Contig Contig position Allele
Function mRNA Protein
mRNA to Chr Accession Position Allele change Accession Position Residue change
on assembly: is labeled at position on chromosome .

GeneView via analysis of contig annotation: N/A.

GeneView via direct blast against RefSeq sequences (used when no gene model is available):

Function Chr mRNA Protein
SNP to mRNA Accession Position Allele change Accession Position Residue change
on assembly: is labeled at position on chromosome .

GeneView via direct blast against RefSeq sequences (used when no gene model is available): N/A


  Integrated Maps: back to top
Genome Build Chr Chr Pos Contig Contig Pos SNP to
Chr		 Contig
allele		 Group term Group label Contig label Neighbor
SNP		 Map Method
doesn't map to any assembly.

  NCBI Resource Links back to top
Resource
Submitter-Referenced
GenBank
NC_000007.11
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss# Population Individual
Group		 Chrom.
Sample Cnt.
 Source C/T
 T/T
 HWP C
 T
ss69022741 HapMap-CEU European 120 GF 1.000 1.000
HapMap-HCB Asian 90 GF 1.000 1.000
HapMap-JPT Asian 90 GF 1.000 1.000
HapMap-YRI Sub-Saharan African 120 GF 0.050 0.950 0.025 0.975

Summary Average
Het.+/- std err:		 Individual
Count		 Founders
Count		 Individual
Overlap		 Genotype
Conflict
0.014+/-0.083 0 0 0 0

  Validation Summary: back to top
Validation status Marker displays
Mendelian segregation		 PCR results confirmed
in multiple reactions		 Homozygotes detected
in individual genotype data
byClusterbyFreq UNKNOWN UNKNOWN UNKNOWN

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Revised: May 25, 2006 1:38 PM .