|
|
| ID |
SNP51.114 |
| OMIM_ID |
ccaaaaaacaaaacagcttatgagcacctc
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs41298856
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/CAAA
|
| Orientation |
T-box1 |
| Chr-Number |
chromosome 22 |
| SNP
type |
fwd/ |
| Length |
N |
| 5'
Near Seq 30 bp |
511 |
| 3'
Near Seq 30 bp |
cctggtctcttaaaagaaaaaacaaacaaa |
| Fasta
Sequence |
>gnl|dbSNP|rs41298856|allelePos=256|totalLen=511|taxid=9606|snpclass=2|alleles='-/CAAA'|mol=Genomic|build=127
AGTCAGGAGG TCAAGTGTGC ATGCAAGAGG TGGCAGGGGA CAGATGTGCT GCTGTTCCCA
GGCCACCTGC ACAGCTGGAT GGTGGAAGCA GTTCACTTAA AGGCCATGAG TTACTCGGGA
GGCTGAGGCA GGAGGATCAC TTGAGCCTAT TAGTTGGAGG CTGCAGTAAG CTATGATCAT
GCCACTGCAC TCCAGCCTGG GTGACAGAGT GAGACCCCCA CTGTCCCTGG TCTCTTAAAA
GAAAAAACAA ACAAA
N
CCAAAAAACA AAACAGCTTA TGAGCACCTC CTACTAATTT CCTCAGCTTA GCACACCCTG
TGGCCGTTGT CCCCATCGTC CGTGGCTTCA TCCCTCAACT GATGCTTTCC TATGTGGACT
TCCCGGCCAG TGCTGTGGGA CCTCCCCTGT AGGGCTGGCC AGCCTCATGG GCTGGGCTAC
CCGTCCCACT CAGCAGTGGC TGCCTGGCCT CCCCTCTGTC CCTCCTGCCC AGCTCCTAAT
GGGCCTCCCA TAAAA
|
|
|
