|
|
| ID |
SNP51.311 |
| OMIM_ID |
gtgggcttccttggaggaccctccctccag
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs2238779
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
T-box1 |
| Chr-Number |
chromosome 22 |
| SNP
type |
fwd/B |
| Length |
Y |
| 5'
Near Seq 30 bp |
511 |
| 3'
Near Seq 30 bp |
catttccaggtggcccctccagcttggctg |
| Fasta
Sequence |
>gnl|dbSNP|rs2238779|allelePos=256|totalLen=511|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=127
CCGCCACCTC CTGGGAGAGC CTGCAGGGCC CGAGCTCTGG GGACAAGAGC TGCTGCTCAG
GCCCCAGAGG AAGGTCTAGG TGGGAAATGG GCCGCCAGGA GGTGGACACC AACACATAGG
AGCACATCCC AAGACACCCA TCACCCTGTG TGGTGGGTGC TGGAAAGAAA CAGCCTAGTT
ATGAGAGAGA CTTGCAACTG GGGGCACCCT AGCACCCCAC GGAGGCATTT CCAGGTGGCC
CCTCCAGCTT GGCTG
Y
GTGGGCTTCC TTGGAGGACC CTCCCTCCAG GCGGCCAGCC AGAAGGGGCC ATCTCCAGGC
AGGCACCCCC TTCAGGAGAG CCCATGCCCA GTCACTGCCT GGGAAGCTTA CTGCAGGGCT
GGCCCCCACC TGCCACTGTC ACCTCCTGAC CTCCACCTGC TCTCCTGGGT CCTCAGGCCT
CACACAGTCC TGTCCTTCTA ACAGGTGACT GCAGGATGGA GCCCCAGGCA TCTCGGCATC
CTGATGCGGT CACTG
|
|
|
