|
|
| ID |
SNP51.278 |
| OMIM_ID |
tggtcctgctcagagaggaaggaaaggggc
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs8141387
|
| 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 |
401 |
| 3'
Near Seq 30 bp |
tcctgcaggagcagctcctggggacaatgg |
| Fasta
Sequence |
>gnl|dbSNP|rs8141387|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=116
GCTTGGGCAT ACCCTCAGGC TGGGGCACAT GCAGGAGCCC CACCCCCATG CCCCCACCGA
CTGGCCCAGG CCTCTCTGGG TGCAGACTGC CAACACAGGC ACGTCTCCTG CAACACTACC
AAATCTGCGG CCACCAGCAT CCCTACCACC CGCCTCCACG GGACTGTCCT TCCTGCAGGA
GCAGCTCCTG GGGACAATGG
Y
TGGTCCTGCT CAGAGAGGAA GGAAAGGGGC CTGGAACCAG CTGGTCCATC CCCACACAGC
ACTCCTCACT GGACTTGTCC CTGGGTCCCC TCAGTGACAC TGAGAGACAT AAGTCATTGT
CACTGTCATG GCCCAGAATG ACTACTCAGG GCAAGAAAAA TGCACTAAGG ACAGCTTCCC
TTTTCTGACA TGGCCCACAA
|
|
|
