|
|
| ID |
455 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs36225898
|
| 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 |
gaaccacttccatggggaaagggtaaacta |
| 3'
Near Seq 30 bp |
actggagaatgcaaaaaccttttttttttt |
| Fasta
Sequence |
CACTGCACTC CAGTGTGGTG ACAGAGCCAG ACTTCCTCTC AAAAAAACAA ACAAAGGTTC
CAAGGCTCTA CTCCAGAAAT TAAGACCCAT TATGTGTGGG CTGGGCACAG GAATATGTTT
AAATCCCCCC CCACCTCCCC AGGGTGATTC TGCTGCTGAA TTAGGTTTTG GAACCACTTC
CATGGGGAAA GGGTAAACTA
R
ACTGGAGAAT GCAAAAACCT TTTTTTTTTT TTTTTTTTTT TTTGAGACAG AGTCTCACCC
TGTTGCCCAG GCTGGAGTGC AATGGCGCGA CCTCGGCTCA CTGCAACCTC CACCTCCCAG
GTTCAAGGGA TTCTCCTGCC TCAGCCTCCC AAGTAGCTGG GATTACAGGT GCCCACCACT
ACACCCGGCT AATTTTGTGT
|
|
|
