|
|
| ID |
467 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs36022367
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/C
|
| Orientation |
fwd/ |
| Chr-Number |
2 |
| SNP
type |
N |
| Length |
601 |
| 5'
Near Seq 30 bp |
taatatctgggatcacagacgtgggtttta |
| 3'
Near Seq 30 bp |
ccatgttgcccaggatggtgtcaatctcct |
| Fasta
Sequence |
CCAGCTGCGG TGCAGTGGCG TGAACATAGC TGACGGCAGA AGACCTCCTG GGCTCAAACG
ATCCTCCTGG CTCGTGCTCC CAAAGTACTG GGATTATGGC GTGTGACACC ACGCCTGGCG
TCAAACGTTT GTCTTTTTAT TTATTTTATT TTGTATTTTT TGAGACAGGG TTTTCAATCT
GTCGCCCACG CTGGAGTGCA GTGGCACAAT TTACGGCTCA CCGCAGCCTC GACCTCCCGG
GCTCAGGTGA TCCTTTCGCC TCAGCCCTGC TAATATCTGG GATCACAGAC GTGGGTTTTA
N
CCATGTTGCC CAGGATGGTG TCAATCTCCT GGGCTCAAGT GATCCGCCCA CCTCGGCCTC
CCAAATTGCT GGGATTACAG GCGTGAGCTA CCGCGCCCTG CCACAAACGC ATATCTTCTA
ACGTACCATT TCATTTACTT GCTATATTCA TTATCTGAAT TTTCTCATAT TAGAATGTAA
GCAGAATAAA GGCAGTGATT TTTCTTTTTA CTGGCGATCC TCAGAGCCAA GAAGAGTCTG
GGACATAGCA GGCCATATAA ATGTTTTCGA ATGAGTGAAT CATCAACGAG TGGATGAAAC
|
|
|
