|
|
| ID |
SNP51.270 |
| OMIM_ID |
tttttttttttgagacagggtctccctctg
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs11404688
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/T
|
| Orientation |
T-box1 |
| Chr-Number |
chromosome 22 |
| SNP
type |
fwd/T |
| Length |
N |
| 5'
Near Seq 30 bp |
801 |
| 3'
Near Seq 30 bp |
cagggtgtgttgttactcttaatttttttt |
| Fasta
Sequence |
>gnl|dbSNP|rs11404688|allelePos=401|totalLen=801|taxid=9606|snpclass=2|alleles='-/T'|mol=Genomic|build=120
ATGTCCCTAT GAAGGACATG AGCTCTTCAT TTTTTATGGC TGCATAGTAT TCCATGGTGT
ATATGTGCCA CATTTTCTTA ATCCAGTCTA TCGTTGTTGG ACATTTGGGT TGGTTCCAAG
TCTTTGCTAT TGTGAATAGT GCTGCAATAA ACATACGTGT GCATGTGTCT TTATAGCAGC
ATGATTTATA ATCCTTTGGG TATATACCCA GTAATGGGGT GGCTGAGTTC TACTCTTATA
AAGAGCGTGC TGGCCTTTCC CATGCCTTCT CGTCTGTTTT GACCCATTCT GGGTATCGGT
CCTTTTCGTC TCCCCCTCTC CATCCTCTCT CAGCCCCTTT CACTGGGTTT CAGTGTGCTG
GGCACAGGTT CAGGGTGTGT TGTTACTCTT AATTTTTTTT
N
TTTTTTTTTT TGAGACAGGG TCTCCCTCTG CCCCCCAGCC TGGAGTGCAG TGGTATGATC
ATGGCTCACG GCAGCCTTGA CCTCCTAGGC TCAAGTGATC CTCTTACCTC AACCTCCCAT
GTAGCTGGGA ACACAGGCAC GCACCACCAT GCCCGGCTAA TTTTTAAGTT TTTTGTGGAG
ATGGGATTTT GCCATGTTGC TCAGGCTGGT CTCGAACTCC TGAGCTCAAG TGATCCTCTT
GCCTTGGCCT CTCAAAGTGC TGGGATTACA GGCGTGAGCC ACCACACCCA ACCAGGATTT
ATTACTCTTA ACTAGTAAAA CAGCACATTC CTGCTCATTT CAAGAGACAG GATCTTGCTC
TGTCACCCAG GCTGGAGTGC AGTGGCATCG TGATCAAGGC
|
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