SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 67
OMIM_ID 143100
Disease HUNTINGTON DISEASE
Gene

HTT

SNP_ID

rs762855

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 4
SNP type Y
Length 1665
5' Near Seq 30 bp ttttcttgagaaggacagcagagaaacagc
3' Near Seq 30 bp gttagttcccagttcttgggaggctgatgt
Fasta Sequence CGGGGGGTGA TGCAGGCAGA GAGGAGCCCA GTAAAGCCTA CTTTAGCCAG GCCACACCTG CAACCCAGAG TCCCCTGCTC TGTGGCCACA AACAGCACCT CCGCCTTGTC TCAGAGCCTG TCCTAAAGGG AAACCCAGCA TTGTCCCCAG TGGGGTAGCA GTAGCCTCCC TTTTCTTGAG AAGGACAGCA GAGAAACAGC Y GTTAGTtccc agttcttggg aggctgatgt gggaggatca cctgaaccca ggaatttgag gctgcaagtg agctaggatt gcaccactgc actccagctt gggtgataga gcgacactgt ctctaaaaaa aTTAAGTTCC AGCGAggtgc ggtggctcac gcctgtaatc ccagcacttt gggaggccaa ggcaggcaga tcaccagagg tcaggagttc gagaccagcc tggccaacat ggcgaaaccc tgtctctact aaaaatacaa aaattagccg ggtgtagtgg tgcatgcctg tagtcccagc tattccggag gctgaggcag aattgcttga acctgggagg tggaggttgc agtgagccaa gatcatgcca ttgcactcca gcctgggtga caagagtgag actctgtctc aaaaataaat aaataaataa aGTTCCCAGT TCTCTGCTGT TAATAAGGGC CTTTGTCCAC TGTGTCAGGC CTCAAGGTTG TTAGTTACCT CAgtgggcag actcataaga tggccccagc acccctcacc tcctggtatt gacacccttg tatgacccct ccccgtgagc ttgggctgta cctggtggcc tgcttctaac caatgggcaa aggtgatgga atgtcacccc atgactaggt cgcaaaaggg tatgacttca gtctccctgg ccctctctgt tgccttcttg gcatggatgc tctgatgaag tcagctgcca tgttggagag gcccacatgg cgaggacata aaggcggcct ctggccaaca ggcagtgaga actgaggttc tcagtccagc aggccatgag gaactggatc ctgccaacac cacgtgagat tggaaaggga cccttccccg gctgagctct caggtgggag gcagctggta tttgactgaa ccctggcgag aagtggagct ggttaagctg ggtccaaatt cctgacccac agaacgtgtg acgataCATA TGGCTCTACA CGTAACTACA TATAACTCTA TGACTAGACA TGTGTGCTGC CAAGCCACAG TGCTGGGGTG ATTTGTTCCA GCAGCAGATG ACtgtatttg tttacttggg ctgccataac aaagtaccac agaccgggca gcttaaacaa cagaaatgta tcttctcatg gtcctagagg ctagaagtcc gagatgaagg tgttggcaag gttggtttcc cctgagccct gtccttgact tgcagacagc tgcctttctt ggtgtcctca cgtggccgtc cctctgagca tgtccgtgtc ctaatctctt cttgtaagac atcagtcgga ttatggccca ccctaatgat ctcattttag cctccttacc tccttaaaga acctgtctcc aaatacaatc ccattctgag gttctggggc ttaggacatc aacctgaatg agggacacag ttcgtcccat aacaATAAGT AATA
     

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