|
|
| ID |
465 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs756561
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
R |
| Length |
664 |
| 5'
Near Seq 30 bp |
aatctgtcgcccacgctggagtgcagtggc |
| 3'
Near Seq 30 bp |
caatttacggctcaccgcagcctcgacctc |
| Fasta
Sequence |
Ggtgcagtgg cgtgaacata gctgacggca gaagacctcc tgggctcaaa cgatcctcct
ggctcgtgct cccaaagtac tgggattatg gcgtgtgaca ccacgcctgg cgtcaaacgt
ttgtcttttt ATTTAtttta ttttgtattt tttgagacag ggttttcaat ctgtcgccca
cgctggagtg cagtggc
R
caatttacgg ctcaccgcag cctcgacctc ccgggctcag gtgatccttt cgcctcagcc
ctgctaatat ctgggatcac agacgtgggt tttaccatgt tgcccaggat ggtgtcaatc
tcctgggctc aagtgatccg cccacctcgg cctcccaaat tgctgggatt acaggcgtga
gctaccgcgc cctgccACAA ACGCATATCT tctaacgtac catttcattt acttgctata
ttcattatct gaatcttctc atactagaat gtaagcagaa taaaggcagt gatttttctt
tttactggcg atcctcagag ccaagaagag tctgggacat agcaggccat ataaatgttt
tcgaatgagt gaatCATCAA CGAGTGGATG AAACGATAAT GTGGCTAACA GGCAGCAGTA
AGGAGGCTGT GTAGAATAAA CCCGTAATCC CGATGTTGGC AGTTTG
|
|
|
