|
|
| ID |
457 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs36225899
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
R |
| Length |
401 |
| 5'
Near Seq 30 bp |
gcccaggctggagtgcaatggcgcgacctc |
| 3'
Near Seq 30 bp |
gctcactgcaacctccacctcccaggttca |
| Fasta
Sequence |
GTGGGCTGGG CACAGGAATA TGTTTAAATC CCCCCCCACC TCCCCAGGGT GATTCTGCTG
CTGAATTAGG TTTTGGAACC ACTTCCATGG GGAAAGGGTA AACTAAACTG GAGAATGCAA
AAACCTTTTT TTTTTTTTTT TTTTTTTTTG AGACAGAGTC TCACCCTGTT GCCCAGGCTG
GAGTGCAATG GCGCGACCTC
R
GCTCACTGCA ACCTCCACCT CCCAGGTTCA AGGGATTCTC CTGCCTCAGC CTCCCAAGTA
GCTGGGATTA CAGGTGCCCA CCACTACACC CGGCTAATTT TGTGTGTGTT TTTAGTAGAG
ACGGAGGTTC ACCATGTTAG TCAGGCTGGT CTCGAACTCC TGACCTCAGG TGATCTGCCC
GCCTCGGCCT CCCAAAGTGC
|
|
|
