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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs237773          
refSNP ID: rs237773
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_004578.2:c.228-1271C>T
NT_004559.13:g.5632478C>T
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 ss436545 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs237773 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
ss306531KWOK|OVLP-000621-349492rev/BC/Tgttggatgtgggcgaccgcgtggtggctcagcctgtaatcccagcactttgggaggccga06/30/0010/10/0379Genomic97 %
ss436545KWOK|OVLP-000621-342399fwd/TA/Gtcggcctcccaaagtgctgggattacaggctgagccaccacgcggtcgcccacatccaac06/30/0010/10/0385Genomic99 %
ss1005160KWOK|OVLP-000804-130287fwd/TA/Gtcggcctcccaaagtgctgggattacaggctgagccaccacgcggtcgcccacatccaac09/02/0010/10/0389Genomic97 %
ss1686405KWOK|OVLP-000925-292106fwd/TA/Gtcggcctcccaaagtgctgggattacaggctgagccaccacgcggtcgcccacatccaac10/05/0010/10/0389Genomic99 %
ss1730311KWOK|OVLP-000925-303929fwd/TA/Gtcggcctcccaaagtgctgggattacaggctgagccaccacgcggtcgcccacatccaac10/05/0010/10/0389Genomic97 %
ss13032776SC_SNP|NT_031728.8_139125rev/BC/Tgttggatgtggggccacgcgtggtggctcagcctgtaatcccagcactttgggaggccga10/22/0310/31/03119Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs237773|allelePos=849|totalLen=1543|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=119
 GTCACCACAG GAATCCATAG TCACCACGGC CCTACACCCA CCTGCATCCC TGCCCTATTA
 CTACGGGAAA ACTGAGTGTC CCAGTATGTC ATATCCACTC TCACATTCAA GAAGGCGTCT
 TTTGGTCATA CATGTTTTCC CCTACATTGT CAATCTCACC CTCTTTGTGA GATTTTTCCC
 ATTAGTGGCC GGacacctat aatcccagca ctttaggagg cccaggaggg aggactgctt
 gaggccagga gtttgagacc agcctgggta agagagagag accctgtctc tacaaaaaat
 tagccaggta tggcagtaca cacctgtaat cccagctact caggaggctg agacagaagg
 actgtttgat cccaggaatt tgaggtgacg gtgagcgatc atgccactgc actccagccc
 aggcaacaga aagaaaaaaa aaaaaaaGCC AGGAGTTCAG GATTTTTCCT ATTAGCAAAA
 TAAAAATAAA TTGGCTCTGG TACCGCCCAT CTTAAAACAC AAAACAGAAA TATGCTGCAC
 CATCTTTTCA GTTACTGTCC CACTGTCTGC TCTTCTCCAC ATCCAACTGT Cttttttgag
 acagagtttc gctcgttacc caggctagag tgcaatggcg cgatctcagc tctctgcaac
 ctctgcctcc caggttcaag caattctcct gcctcagcct cctgagtagc tgcacccgcc
 accacgcctg gctaattttt gtatttttag tacagacggg gtttccccat gttagccagg
 ctggtctcga actcttgacc tcggatgatc cacccgcctc ggcctcccaa agtgctggga
 ttacaggc
 R
 tgagccacca cgcGGTCGCC CACATCCAAC TTTCTGAAAG AGCTGTCTTT ACCTGCAGCT
 TCCTCTTCTT CACCGCCAAC CTAGTGTCCA TCTCTGCTAC TCCCCAAAAG CCTGTCAAGG
 TCCCCACCCT CTCTGCAACC GAAGCTGGAG TGGGCATTTC TGTCCTCACT CACTCGCGCA
 GCCTCTGCGC CCTGCACTCT GCTAGTCTTC CTCCCGCTCA CCAGCCACTT CTCTGGCTCT
 GGTCATTCTT CTGAATCTGC CCTGCTGAGA TTGCGATTCC CCAGAGCTGG GTCCTGGGCT
 CTCTTAACAT TCGACTCAAA TTTTGTctcc agctcagatc caagtgctgc ctccatatct
 ccatgagact gcctgataaa catgtcaaac ttaacatctg cacagcagga ctctttttgg
 tcccaccctc caggcccgtc ctGGCCTAGG AAGAGGCATC ACCACGCACC CTGTTTCTAA
 AGCAAATCAG CTCCACATTC ATCCTCAATT CCTGTGCACC TCCACATTCA CTCCGCCAGC
 CTAGTGCAGT CTCCTACACT ACACAAATCC TGTGTCTGCC CACGCTGCTG TCCCTGCTGC
 CATGTGTGGC CCACAGTCCA TTCTTCAGAG CAGCCCAACT CATCAAGGCC CAGGACAGGA
 CATCTCCGTC ACTGTACCTG TCCCTTTGGC CCCA

  GeneView back to top
GeneView via analysis of contig annotation: RAB4A RAB4A, member RAS oncogene family
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_004559->NM_004578
svfunction
HuRefNW_001838547->NM_004578
svfunction
CeleraNW_927128->NM_004578
svfunction
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_004559->NM_004578->NP_0045695632478forwardintron
HuRefNW_001838547->NM_004578->NP_004569144331forwardintron
CeleraNW_927128->NM_004578->NP_0045695279810forwardintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs237773 maps exactly once on NCBI human chromosome 1
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
1NW_001838547.1144331199920974minusCalt_assembly_8HuRefHuRefview848
1NW_927128.15279810202698640minusCalt_assembly_1CeleraCeleraview848
1NT_004559.135632478227496947minusCref_assemblyreferencereferenceview848

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_031728 AL117350.12 AL162595.8
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AL117350.12 NC_000001.9 AC036234.4 AC139475.1 AL672289.5

  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
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .