|
|
| ID |
SNP51.292 |
| OMIM_ID |
ttcttaccacaaaaatgagaactatgtcag
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs5992482
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
T-box1 |
| Chr-Number |
chromosome 22 |
| SNP
type |
fwd/T |
| Length |
S |
| 5'
Near Seq 30 bp |
801 |
| 3'
Near Seq 30 bp |
catataaaattgacgtatttattgtgtaaa |
| Fasta
Sequence |
>gnl|dbSNP|rs5992482|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='C/G'|mol=Genomic|build=127
TTTAAACATT GACTGTAAAC TCATTATAAA CACTTCTAAA TATTTAATGG AAACTACAAG
CTTAACATAT CTGATCCAAA AATGCCTTAA ACACCTCAGT ACAGACACCC ACACACTATG
AGGATGATTC CCTCAAACTG GTTCTGAAAG CAGTAGCTGT GCTTTTCTCT ATCGCGTTCT
TATTCTTTCT CCGACGTGCT CTTAGCACCC TCCTGGGGAT TAGCATCCGA CCCACATCAC
TCGGGAAAAG CCCTGGCTGG CGGCTCCCAG GCGGAGGCAC CACGGTGAGG CCAAGTGCTG
CTGTCCAGTA AGCCTGACTG CCCCCTCAGG CTCTTTCCCT TCACATTTAC TTATTTATTT
TTTAAATCGA CATATAAAAT TGACGTATTT ATTGTGTAAA
S
TTCTTACCAC AAAAATGAGA ACTATGTCAG GTGATGTATT TGCTAGTTAG CTAGACTTAA
GCAGGCCTTT AGTTTTCAGt ttttaacatt gagggaaaat acacgtaaat caaatttacc
atcgtagccc tttgtaagtg tacatttcag tggcatgaag tccatccaca tgactgtgca
gccatcacca ccagccatct cagaactctt catctcagaa aactgaaact ctgtccccat
taaacaagaa ctcctcattc ccctcccctg gcagccagca ttctactctc tgtctctgtg
aatctgacta ctctaggcgc ctcatgtaag tggaatcaca cagcatttgt ctttttgtgg
ctggcttagt tcactgagtg taaggacctc aaggttcatc
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