|
|
| ID |
478 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs34355730
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
R |
| Length |
167 |
| 5'
Near Seq 30 bp |
gccgtggccggacgccgctcgggggacgtg |
| 3'
Near Seq 30 bp |
gaggggaggcgggaaacagcttagtgggtg |
| Fasta
Sequence |
CTTATGATTG GTTGCCGCGG CAGACTCCCA CCCACCGAAA CGCAGCCCTG GAAGCTGATT
GGGTGTGGTC GCCGTGGCCG GACGCCGCTC GGGGGACGTG
R
GAGGGGAGGC GGGAAACAGC TTAGTGGGTG TGGGGTCGCG CATTTTCTTC AACCAGGAGG
TAGGAG
|
|
|
