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BUILD 130
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Reference SNP(refSNP) Cluster Report: rs421206          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:80/130
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:G/T
Ancestral Allele:T
Clinical Association:unknown
HGVS Names
NM_001077181.1:c.544A>C
NM_003671.3:c.655A>C
NM_033331.2:c.655A>C
NP_001070649.1:p.Ile182Leu
NP_003662.1:p.Ile219Leu
NP_201588.1:p.Ile219Leu
NR_003595.1:c.677A>C
Links , Linkout

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 ss555773 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs421206 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
ss555773SC_JCM|AC006024.1_67170fwd/BG/Tcacagaaggcaataaatcggtctggtattaccaatttaaatctccgttttctgctttttc07/12/0010/10/0380Genomicunknown
ss24811469SEQUENOM|sqnm198651byFreqfwd/BG/Tcacagaaggcaataaatcggtctggtattaccaatttaaatctccgttttctgctttttc06/18/0408/05/04123cDNAunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs421206|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='G/T'|mol=Genomic|build=123
 AAAGAAAAGA TCATGGTGAT CGAAGCCAGC ATCCGTAAAG CGTTTGGCAT CATACATCCT
 TTTATTCAGA CGAATAATGG TAGTAACATT GTGATTCTTA AAATATTGAA TATAAGTCTC
 GGGAGAATGT TGGTGGTAAC CACTTTCAAG TCTGGCTCTT GAATGAGGTC CACAGAAGGC
 AATAAATCGG TCTGGTATTA
 K
 CCAATTTAAA TCTCCGTTTT CTGCTTTTTC ATAGTGTTCA TATTCATCAA GGTTAAATGA
 GTTGAAATTA AGGAAGCCAT ACTGCATTGC CTTCTTTACT GCATGAAAAC AGTCAAGAAG
 TGTAATGTAG AAATTGCAGC TTCCATAGGC AGCATCTCTG AAAGGAATAT AGGGTGTATC
 TCCAAAGATT AATATTCTAT

  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
dbSTS GenBank
sqnm198651 AC006024 AC004899
dbSNP Blast Analysis
UniGene Cluster ID
546513

  Population Diversity back to top

Sample AscertainmentGenotypesAlleles
ss# Population Individual
Group
Chrom.
Sample Cnt.
Source HWP G
T
ss24811469 CEPH 184 AF 0.520 0.480

Summary Average
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.499+/-0.020 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
byFreq UNKNOWN UNKNOWN UNKNOWN

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Revised: May 25, 2006 1:38 PM .