|
|
| ID |
SNP51.276 |
| OMIM_ID |
tggggaccatccacacccccttcacaccac
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs9606155
|
| 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 |
601 |
| 3'
Near Seq 30 bp |
ggaaatagatagattcttgactaagcgggg |
| Fasta
Sequence |
>gnl|dbSNP|rs9606155|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=127
TGCCCCTTCT GTAAGCTGCT GTGATGGGCA GTATGGTGTA GGGGATAGGG GGCTCGTCCC
ACCGCTGTTC CCCCACAGGC TCCCCCTCAG CTGTTGGACT TCCCCCAAAC ATCCTCCTCC
AGGTTCCCTA GCTGGTCCAG AGGCCCCGTT GCCCTCCCCT AGCCTGGCTG CAGACGTCCA
GCTGCCAGGA CTCAGGAGGA CGAGAGACCA GAAGGGCCCC CAGACTCCTC ACTCCCAAAA
ACTCTCCAAA AACAACAGAT GCACAACGCA GGAAATAGAT AGATTCTTGA CTAAGCGGGG
R
TGGGGACCAT CCACACCCCC TTCACACCAC TGCATCCCAC GGAAGGGTTC TAGGACCCCA
GGGCCTGGGG GTGCAGCTGG ACGATCCTGC AGTAGCCCCG CTCCCTGTTT TCAGAAGACC
CCCCCACGGC TGCCCTCTGC AGCATGTGCC CCTTTGTCGA AGGGACAATG GGCACTCCAT
TGCCCAGAGA GGCTTCTCAC CCAGGAAAGC ACTGGAGGTG CAGAGGCAGG AGCACGCGGG
GGCTTGGCTG CGGGACAAGG CGAGTCTGTT TGGTGGCACC TTGAGCTGCG GAGGAAGACA
|
|
|
