|
|
| ID |
464 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs36225562
|
| 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 |
gccgtaaattgtgccactgcactccagcgt |
| 3'
Near Seq 30 bp |
ggcgacagattgaaaaccctgtctcaaaaa |
| Fasta
Sequence |
CTCACGCCTG TAATCCCAGC AATTTGGGAG GCCGAGGTGG GCGGATCACT TGAGCCCAGG
AGATTGACAC CATCCTGGGC AACATGGTAA AACCCACGTC TGTGATCCCA GATATTAGCA
GGGCTGAGGC GAAAGGATCA CCTGAGCCCG GGAGGTCGAG GCTGCGGTGA GCCGTAAATT
GTGCCACTGC ACTCCAGCGT
R
GGCGACAGAT TGAAAACCCT GTCTCAAAAA ATACAAAATA AAATAAATAA AAAGACAAAC
GTTTGACGCC AGGCGTGGTG TCACACGCCA TAATCCCAGT ACTTTGGGAG CACGAGCCAG
GAGGATCGTT TGAGCCCAGG AGGTCTTCTG CCGTCAGCTA TGTTCACGCC ACTGCACCGC
AGCTGGGGCG ACAGAGCGAG
|
|
|
