|
|
| ID |
SNP51.248 |
| OMIM_ID |
cggcatggatcccatggccgactatatgct
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs28939675
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/T
|
| Orientation |
T-box1 |
| Chr-Number |
chromosome 22 |
| SNP
type |
fwd/ |
| Length |
W |
| 5'
Near Seq 30 bp |
511 |
| 3'
Near Seq 30 bp |
ggatgtttcccaccttccaagtgaagctct |
| Fasta
Sequence |
>gnl|dbSNP|rs28939675|allelePos=251|totalLen=501|taxid=9606|snpclass=1|alleles='A/T'|mol=cDNA|build=125
CCGCCGCCGC ACGCCTACCC GTTTGCGCCG GCCGCCGGGG CCGCCACCAG CGCCGCCGCC
GAGCCCGAGG GCCCCGGGGC CAGCTGCGCG GCCGCAGCCA AGGCGCCGGT GAAGAAGAAC
GCGAAGGTGG CCGGTGTGAG CGTGCAGCTA GAGATGAAGG CGCTGTGGGA CGAGTTCAAC
CAGCTGGGCA CCGAGATGAT CGTCACCAAG GCCGGCAGGC GGATGTTTCC CACCTTCCAA
GTGAAGCTCT
W
CGGCATGGAT CCCATGGCCG ACTATATGCT GCTCATGGAC TTCGTGCCGG TGGACGATAA
GCGCTACCGG TACGCCTTCC ACAGCTCCTC CTGGCTGGTG GCGGGGAAGG CCGACCCTGC
CACGCCAGGC CGCGTGCACT ACCACCCGGA CTCGCCTGCC AAGGGCGCGC AGTGGATGAA
GCAAATCGTG TCCTTCGACA AGCTCAAGCT GACCAACAAC CTACTGGACG ACAACGGCCA
CATTATTCTG
|
|
|
