|
|
| ID |
448 |
| OMIM_ID |
219700
|
| Disease |
CYSTIC FIBROSIS |
| Gene |
TGFB1
|
| SNP_ID |
rs5828099
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/G
|
| Orientation |
fwd/T |
| Chr-Number |
19 |
| SNP
type |
N |
| Length |
801 |
| 5'
Near Seq 30 bp |
tatggtgactgaatgagttcattaatgtaa |
| 3'
Near Seq 30 bp |
gcacttcaacagtgcccaaggtgctcaata |
| Fasta
Sequence |
AGtcagggct cactgcagcc ttgacctccc aggatcaagt gatcctccca ccttagcctc
cagagtagct gggaccacag gtgtacattt tttaaaagtg ttttgtagag atagggtctc
actatgttac ccaggctggt ctcaaatgcc tggattcaag taatcctccc atctctgcct
cccaaaagtg ctaggattac aggcgtgagc caccccgcct ggccTGAACT ACTATCTTTT
ATTGTCTTCT TCACTATCCC CCACTAAAGC AGGTTCCTGG TGGGCAGGAA CTCCTCCctt
aacctctctg ggcttgtttc ctcaccttta aaatgggtgt tatcagagtc cctgcatctc
agagtgttgc tatggtgact gaatgagttc attaatgtaa
N
gcacttcaac agtgcccaag gtgctcaata aatAGATCTA ACTACAGTAG TGTTCCCCAC
TGGTCCCCTG TGCCTTGATG CCGGGCAAAG GAATAGTGCA GACAGGCagg aggaggcaga
gagggagaga gagggagtgg gagtggggga acgtcaggga TGGAGACCCC AGGCAGGCGC
CCAATGACAC AGAGATCCGC AGTCCTCTCT CCATCTTTAA TGGGGCCCCA GGTGGGCTTG
GGGCACGGGT GTCCTTAAAT ACAGCCCCCA TGGGCAAGGC AGCGggggcg gggcggggtg
gggccgggcc tgccggggcg gggcggggcg gggcgggACC TCAGCTGCAC TTGCAGGAGC
GCACGATCAT GTTGGACAGC TGCTCCACCT TGGGCTTGCG
|
|
|
