|
|
| ID |
463 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17217674
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/C
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
M |
| Length |
511 |
| 5'
Near Seq 30 bp |
ttattttgtattttttgagacagggttttc |
| 3'
Near Seq 30 bp |
atctgtcgcccacgctggagtgcagtggca |
| Fasta
Sequence |
ATTTTAAAAT TTCAACCTTC CTCTTCCTTA ACTGGTCTTC CCCTACCCCC CCTCAAGACG
GGGTCTCTCG CTCTGTCGCC CCAGCTGCGG TGCAGTGGCG TGAACATAGC TGACGGCAGA
AGACCTCCTG GGCTCAAACG ATCCTCCTGG CTCGTGCTCC CAAAGTACTG GGATTATGGC
GTGTGACACC ACGCCTGGCG TCAAACGTTT GTCTTTTTAT TTATTTTATT TTGTATTTTT
TGAGACAGGG TTTTC
M
ATCTGTCGCC CACGCTGGAG TGCAGTGGCA CAATTTACGG CTCACCGCAG CCTCGACCTC
CCGGGCTCAG GTGATCCTTT CGCCTCAGCC CTGCTAATAT CTGGGATCAC AGACGTGGGT
TTTACCATGT TGCCCAGGAT GGTGTCAATC TCCTGGGCTC AAGTGATCCG CCCACCTCGG
CCTCCCAAAT TGCTGGGATT ACAGGCGTGA GCTACCGCGC CCTGCCACAA ACGCATATCT
TCTAACGTAC CATTT
|
|
|
