SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID SNP51.007
OMIM_ID tgttccctccttagtgactttatttgctgt
Disease DIGEORGE SYNDROME
Gene

TBX1(T-box1)

SNP_ID

rs61427853

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/G
Orientation T-box1
Chr-Number chromosome 22
SNP type fwd/T
Length R
5' Near Seq 30 bp 401
3' Near Seq 30 bp atttcccctgccggcctagcccaggcccgc
Fasta Sequence >gnl|dbSNP|rs61427853|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=129 GACTTGGGCC TGCGCCCTGG CCTGTTTTCG GGACAGATGC TTGTGCTTTT CCATGGAAGC TGGGAAGAAG GGTCATGACA GACACTGCCG GTCGGTGCTG GGAGGGGGAG AAGCCCCTGA CCGGGATGGG GTCATGGAAA GACAAAAACA GGCAGCACTG TTCTGCTAGC ATTTCCCCTG CCGGCCTAGC CCAGGCCCGC R TGTTCCCTCC TTAGTGACTT TATTTGCTGT GAGTGTCCCT ACGGAGTGAC CTGGCCAGGG GGCACAATGA CAGTAGCCAT GAGTCATCTT GAGACCTGTG TATGAAGCAT TTTTCCCAGG CCAGGTGGCT AAGGGACCTC TCCCCGTTAA CTCAACACCA GGGATGGGGC GAGAGGAACT CTTTGATCCC TCCCTTCCTG
     

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