|
|
| ID |
471 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17217695
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
S |
| Length |
511 |
| 5'
Near Seq 30 bp |
aaggcagtgatttttctttttactggcgat |
| 3'
Near Seq 30 bp |
ctcagagccaagaagagtctgggacatagc |
| Fasta
Sequence |
GCCCTGCTAA TATCTGGGAT CACAGACGTG GGTTTTACCA TGTTGCCCAG GATGGTGTCA
ATCTCCTGGG CTCAAGTGAT CCGCCCACCT CGGCCTCCCA AATTGCTGGG ATTACAGGCG
TGAGCTACCG CGCCCTGCCA CAAACGCATA TCTTCTAACG TACCATTTCA TTTACTTGCT
ATATTCATTA TCTGAATCTT CTCATATTAG AATGTAAGCA GAATAAAGGC AGTGATTTTT
CTTTTTACTG GCGAT
S
CTCAGAGCCA AGAAGAGTCT GGGACATAGC AGGCCATATA AATGTTTTCG AATGAGTGAA
TCATCAACGA GTGGATGAAA CGATAATGTG GCTAACAGGC AGCAGTAAGG AGGCTGTGTA
GAATAAACCC GTAATCCCGA TGTTGGCAGT TTGCTTAGAA AGAAAAAGGG AGGCAGTCGG
AGAGGGGCAC ACGTTTTAAC AAAATACTGG GAGGAGGAGG AAGGCTAGTT TTTTTTTTGT
TTTCAAGTTT CCTTC
|
|
|
