|
|
| ID |
477 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17217709
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
2 |
| SNP
type |
Y |
| Length |
511 |
| 5'
Near Seq 30 bp |
gccctggaagctgattgggtgtggtcgccg |
| 3'
Near Seq 30 bp |
ggccggacgccgctcgggggacgtgggagg |
| Fasta
Sequence |
CCCACCTGGT GGCAACCTAC CCTTGCATAC ACCCCACCCA GGGGCTTCAA GCCTTGCAGC
TGAGTAAACA CAGAAAGGAG CTCTACTAAG GATGCGCGTC TGCGGGTTTC CGCGCGACCT
AGGCGCAGGC ATGCGCAGTA GCTAAAGTCA CCAGCGTGCG CGGGAAGCTG GGCCGCGTCT
GCTTATGATT GGTTGCCGCG GCAGACTCCC ACCCACCGAA ACGCAGCCCT GGAAGCTGAT
TGGGTGTGGT CGCCG
Y
GGCCGGACGC CGCTCGGGGG ACGTGGGAGG GGAGGCGGGA AACAGCTTAG TGGGTGTGGG
GTCGCGCATT TTCTTCAACC AGGAGGTGAG GAGGTTTCGA CATGGCGGTG CAGCCGAAGG
AGACGCTGCA GTTGGAGAGC GCGGCCGAGG TCGGCTTCGT GCGCTTCTTT CAGGGCATGC
CGGAGAAGCC GACCACCACA GTGCGCCTTT TCGACCGGGG CGACTTCTAT ACGGCGCACG
GCGAGGACGC GCTGC
|
|
|
