|
|
| ID |
SNP51.307 |
| OMIM_ID |
tatcggtccttttcgtctccccctctccat
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs4819843
|
| 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 |
801 |
| 3'
Near Seq 30 bp |
tgccttctcgtctgttttgacccattctgg |
| Fasta
Sequence |
>gnl|dbSNP|rs4819843|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=129
gtccgtgtgt tctcattgtt caattcccac ctatgagtga gaacatgcgg tgtttggttt
tttgtccttg cgatagtttg ctgagaatga tggtttccag tttcatccat gtccctatga
aggacatgag ctcttcattt tttatggctg catagtattc catggtgtat atgtgccaca
ttttcttaat ccagtctatc gttgttggac atttgggttg gttccaagtc tttgctattg
tgaatagtgc tgcaataaac atacgtgtgc atgtgtcttt atagcagcat gatttataat
cctttgggta tatacccagt aatggggtgg ctgagtTCTA CTCTTATAAA GAGCGTGCTG
GCCTTTCCCA TGCCTTCTCG TCTGTTTTGA CCCATTCTGG
R
TATCGGTCCT TTTCGTCTCC CCCTCTCCAT CCTCTCTCAG CCCCTTTCAC TGGGTTTCAG
TGTGCTGGGC ACAGGTTCAG GGTGTGTTGT TACTCTTAAt tttttttttt ttttttttga
gacagggtct ccctctgccc cccagcctgg agtgcagtgg tatgatcatg gctcacggca
gccttgacct cctaggctca agtgatcctc ttacctcaac ctcccatgta gctgggaaca
caggcacgca ccaccatgcc cggctaattt ttaagttttt tgtggagatg ggattttgcc
atgttgctca ggctggtctc gaactcctga gctcaagtga tcctcttgcc ttggcctctc
aaagtgctgg gattacaggc gtgagccacc acacccaacc
|
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