|
|
| ID |
466 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs36225894
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
G/T
|
| Orientation |
fwd/B |
| Chr-Number |
2 |
| SNP
type |
K |
| Length |
401 |
| 5'
Near Seq 30 bp |
acgtctgtgatcccagatattagcagggct |
| 3'
Near Seq 30 bp |
aggcgaaaggatcacctgagcccgggaggt |
| Fasta
Sequence |
AAATTCAGAT AATGAATATA GCAAGTAAAT GAAATGGTAC GTTAGAAGAT ATGCGTTTGT
GGCAGGGCGC GGTAGCTCAC GCCTGTAATC CCAGCAATTT GGGAGGCCGA GGTGGGCGGA
TCACTTGAGC CCAGGAGATT GACACCATCC TGGGCAACAT GGTAAAACCC ACGTCTGTGA
TCCCAGATAT TAGCAGGGCT
K
AGGCGAAAGG ATCACCTGAG CCCGGGAGGT CGAGGCTGCG GTGAGCCGTA AATTGTGCCA
CTGCACTCCA GCGTGGGCGA CAGATTGAAA ACCCTGTCTC AAAAAATACA AAATAAAATA
AATAAAAAGA CAAACGTTTG ACGCCAGGCG TGGTGTCACA CGCCATAATC CCAGTACTTT
GGGAGCACGA GCCAGGAGGA
|
|
|
