|
|
| ID |
SNP51.296 |
| OMIM_ID |
agagtgacagagggtctcaaggactctcca
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs5748422
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
T-box1 |
| Chr-Number |
chromosome 22 |
| SNP
type |
fwd/B |
| Length |
Y |
| 5'
Near Seq 30 bp |
801 |
| 3'
Near Seq 30 bp |
agccacagctcgctgacctggggaagctga |
| Fasta
Sequence |
>gnl|dbSNP|rs5748422|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=127
gcagtaagct atgatcatgc cactgcactc cagcctgggt gacagagtga gacccccact
gtccctggtc tcttaaaaga aaaaacaaac aaacaaacca aaaaACAAAA CAGCTTATGA
GCACCTCCTA CTAATTTCCT CAGCTTAGCA CACCCTGTGG CCGTTGTCCC CATCGTCCGT
GGCTTCATCC CTCAACTGAT GCTTTCCTAT GTGGACTTCC CGGCCAGTGC TGTGGGACCT
CCCCTGTAGG GCTGGCCAGC CTCATGGGCT GGGCTACCCG TCCCACTCAG CAGTGGCTGC
CTGGCCTCCC CTCTGTCCCT CCTGCCCAGC TCCTAATGGG CCTCCCATAA AAGCTGATGC
GTGGGAGCCA AGCCACAGCT CGCTGACCTG GGGAAGCTGA
Y
AGAGTGACAG AGGGTCTCAA GGACTCTCCA CCCACAAGGC GGGAATGGGG ATGCTGGCAA
ATCTGGTATG AAGGTTGAGA CCCCGAGGAG AGGCAGGCCT GGGGGACCGT GCAGCAGCTG
TGCCCACCTA GGACCACAGG GCTGGTGGGG CTGGCAGCTT GGTAGAGGGC AGGTGCACAG
CAAAGTTTTC ACCGGTGCCG GCTTGTTGTC TTCCACGCTG GGATTTCACA TGAAGTTCTA
GCTAATTGAG TATAAGCATT TCTAAAGAAC CCCCGGAGGG TTGTTTTTCT TTGTGCAAAC
ACTCCTTTTG TGCAGAGGGT GTTCTGTGGC TTCTTGGCAG AGACACAGGT GGGAAACACC
TGATTGAACA TCATTGCCTG GGGAGTGGAG ACACGCACAG
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