Genome Browser


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SNP Information

dbSNP ID  rs1800708
JSNP ID  IMS-JST035225
Chromosome  6
Chromosome Position  26201282
Strand  +
Allele  C/T
Validation Class  SNP: single nucleotide polymorphism
SNP Effect  POLYPHEN  SIFT

Gene Information

Type mRNA Accession Gene Strand mRNA_Pos Codon_Pos Protein_Pos Allele Codons AminoAcid
 Intron  NM_000410  HFE  +  -  -  -  C/T    -
 Intron  NM_139003  HFE  +  -  -  -  C/T    -
 Intron  NM_139002  HFE  +  -  -  -  C/T    -
 Intron  NM_139005  HFE  +  -  -  -  C/T    -
 Intron  NM_139006  HFE  +  -  -  -  C/T    -
 Intron  NM_139007  HFE  +  -  -  -  C/T    -
 Intron  NM_139008  HFE  +  -  -  -  C/T    -
 Intron  NM_139009  HFE  +  -  -  -  C/T    -
 Intron  NM_139004  HFE  +  -  -  -  C/T    -
 Intron  NM_139010  HFE  +  -  -  -  C/T    -
 Intron  NM_139011  HFE  +  -  -  -  C/T    -

Disease Information

Disease Hit  0
Disease Name  -
Others  -

Disease Information

dbSNP JSNP ALFRED
 
TC
0.3300.669
  
 
TC
0.3300.669
  
  -

Flanking Sequence

dbSNP
>gnl|dbSNP|rs1800708 rs=1800708|pos=201|len=401|taxid=9606|mol=genomic|class=1|alleles=C/T|build=126
CTTGGCTGTACCCCCTGGGGAAGAGCAGAGATATACGTGCCAGGTGGAGC
ACCCAGGCCTGGATCAGCCCCTCATTGTGATCTGGGGTATGTGACTGATG
AGAGCCAGGAGCTGAGAAAATCTATTGGGGGTTGAGAGGAGTGCCTGAGG
AGGTAATTATGGCAGTGAGATGAGGATCTGCTCTTTGTTAGGGGGTGGGC
Y
GAGGGTGGCAATCAAAGGCTTTAACTTGCTTTTTCTGTTTTAGAGCCCTC
ACCGTCTGGCACCCTAGTCATTGGAGTCATCAGTGGAATTGCTGTTTTTG
TCGTCATCTTGTTCATTGGAATTTTGTTCATAATATTAAGGAAGAGGCAG
GGTTCAAGTGAGTAGGAACAAGGGGGAAGTCTCTTAGTACCTCTGCCCCA 
JSNP
>gnl|dbSNP|rs1800708 rs=1800708|pos=201|len=401|taxid=9606|mol=genomic|class=1|alleles=C/T|build=126
CTTGGCTGTACCCCCTGGGGAAGAGCAGAGATATACGTGCCAGGTGGAGC
ACCCAGGCCTGGATCAGCCCCTCATTGTGATCTGGGGTATGTGACTGATG
AGAGCCAGGAGCTGAGAAAATCTATTGGGGGTTGAGAGGAGTGCCTGAGG
AGGTAATTATGGCAGTGAGATGAGGATCTGCTCTTTGTTAGGGGGTGGGC
Y
GAGGGTGGCAATCAAAGGCTTTAACTTGCTTTTTCTGTTTTAGAGCCCTC
ACCGTCTGGCACCCTAGTCATTGGAGTCATCAGTGGAATTGCTGTTTTTG
TCGTCATCTTGTTCATTGGAATTTTGTTCATAATATTAAGGAAGAGGCAG
GGTTCAAGTGAGTAGGAACAAGGGGGAAGTCTCTTAGTACCTCTGCCCCA