|
|
| ID |
459 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs36225896
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
2 |
| SNP
type |
Y |
| Length |
401 |
| 5'
Near Seq 30 bp |
ctgccccctccacctcccaggttcaagaga |
| 3'
Near Seq 30 bp |
tctcctgcctcagcctctcgagtagctgtg |
| Fasta
Sequence |
GATTACAGGC GTGAGCCACC GCGCCCGGCC AGCAAAAACC TTTTCTAAGA GTTAATTTTG
CAGGATGGAT CCTGAGCTCC TTCAGGTGTT TGATAACATT TTATTTATTT TTTGAGACAG
AGTCTCGCTC TGTCACCGAG GCTGGAGTGT AGTGGCGCGA TCTTCGCTCA CTGCCCCCTC
CACCTCCCAG GTTCAAGAGA
Y
TCTCCTGCCT CAGCCTCTCG AGTAGCTGTG ATTACAGGCG CCCACCACTA TGCCCGGTAA
TTTTTGTATT TTTAGTAGAG ACGGGGTTTC GCCATGTTGG CCAGGCTGGT CTCAAACTCC
GGACCTCAGG TGATCCACCC GCGTTGGCCT CCCAATACGC TGGGATTACA GGCGTGAGCC
ACTGCGCCTG GCTGTTTGCT
|
|
|
