|
|
| ID |
456 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs35385590
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/T
|
| Orientation |
fwd/ |
| Chr-Number |
2 |
| SNP
type |
N |
| Length |
601 |
| 5'
Near Seq 30 bp |
gggtaaactaaactggagaatgcaaaaacc |
| 3'
Near Seq 30 bp |
ttttttttttttttttttttttttgagaca |
| Fasta
Sequence |
CACACCTGTA GTCATAGCTA CTTGGGAAGC TGAGGCAGGA GGATCGCCTG AACCCGGGAG
GCAGTGAGCC GAGATTGCGC CACTGCACTC CAGTGTGGTG ACAGAGCCAG ACTTCCTCTC
AAAAAAACAA ACAAAGGTTC CAAGGCTCTA CTCCAGAAAT TAAGACCCAT TATGTGTGGG
CTGGGCACAG GAATATGTTT AAATCCCCCC CCACCTCCCC AGGGTGATTC TGCTGCTGAA
TTAGGTTTTG GAACCACTTC CATGGGGAAA GGGTAAACTA AACTGGAGAA TGCAAAAACC
N
TTTTTTTTTT TTTTTTTTTT TTTTGAGACA GAGTCTCACC CTGTTGCCCA GGCTGGAGTG
CAATGGCGCG ACCTCGGCTC ACTGCAACCT CCACCTCCCA GGTTCAAGGG ATTCTCCTGC
CTCAGCCTCC CAAGTAGCTG GGATTACAGG TGCCCACCAC TACACCCGGC TAATTTTGTG
TGTGTTTTTA GTAGAGACGG AGGTTCACCA TGTTAGTCAG GCTGGTCTCG AACTCCTGAC
CTCAGGTGAT CTGCCCGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCG
|
|
|
