|
|
| ID |
SNP51.295 |
| OMIM_ID |
ggtggggtggccaggagagattatgcaggg
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs5844397
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/A
|
| Orientation |
T-box1 |
| Chr-Number |
chromosome 22 |
| SNP
type |
fwd/T |
| Length |
N |
| 5'
Near Seq 30 bp |
801 |
| 3'
Near Seq 30 bp |
ggaactctggatcctggagctgggccggaa |
| Fasta
Sequence |
>gnl|dbSNP|rs5844397|allelePos=401|totalLen=801|taxid=9606|snpclass=2|alleles='-/A'|mol=Genomic|build=129
TGGACGATAA GCGCTACCGG TGAGCGAGTG GTTGTAAGCG TGAGGGACCG GGAGGGCACC
CTGGAAAGTG GCGGGTCTCC GCCTGGTGAC CCAACTCCAA GGGTCGTCTG CACCATGAAA
CTCTTTAGGC ACCTGCGATG CTGCCCGATC AACCCGCTCC CTCCTCCACT CCCATCTGAC
CCCAGACCCA CAACCCTACT CCATGCCCTC TCAGAACCCG CCTCTGGAGC CGCAGGCTGC
AGACAGCTCT TGCTCCCCTG GGCTGGTGTG GCCCTAGGGT GGTCAGCCAA GTACTCAGCC
CCGGACTTCT TCAAGTCTCC CTCTCCCAGG AGGCCGGCCT GAGCGCCTAG TCCCCTTCCC
CCATCCCCAG GGAACTCTGG ATCCTGGAGC TGGGCCGGAA
N
GGTGGGGTGG CCAGGAGAGA TTATGCAGGG CGGGCCTCAG CTGCCCGGAC AATTAACAGC
AATTAATAAA GAGAACGCGC ACTGCCCTGT GCCTGAGGCC CGGCAAGGCC AAGTGTGGGC
TCCCACCGCA GCGGCACCGG GGCGGGAGGA CCCGCATCCA GCGAAATGAG ATGGCAGGAG
CCCAGCCTCC CCCTCTCGGT GCCCCACAGG GTGTCCAGTT CCTTGATTGT TTTGAGTGTT
GGGGTGGGTG GGAGTTCTCT GTTTAGTCCA TAGTCCCCCT TGGAAAAGCT CCCAGCACAT
GCGGCAGCAG AGGGTTCAAT CTCACAGGTG GGGAAACTTC TCAAAGGCAC TTTTAGGGTT
CGCCCAGCAC ACGGGTCAAG GCCCTCTGGG TTCACCTCCA
|
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