|
|
| ID |
460 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs36225897
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/ |
| Chr-Number |
2 |
| SNP
type |
S |
| Length |
401 |
| 5'
Near Seq 30 bp |
agctgtgattacaggcgcccaccactatgc |
| 3'
Near Seq 30 bp |
cggtaatttttgtatttttagtagagacgg |
| Fasta
Sequence |
ATTTTGCAGG ATGGATCCTG AGCTCCTTCA GGTGTTTGAT AACATTTTAT TTATTTTTTG
AGACAGAGTC TCGCTCTGTC ACCGAGGCTG GAGTGTAGTG GCGCGATCTT CGCTCACTGC
CCCCTCCACC TCCCAGGTTC AAGAGATTCT CCTGCCTCAG CCTCTCGAGT AGCTGTGATT
ACAGGCGCCC ACCACTATGC
S
CGGTAATTTT TGTATTTTTA GTAGAGACGG GGTTTCGCCA TGTTGGCCAG GCTGGTCTCA
AACTCCGGAC CTCAGGTGAT CCACCCGCGT TGGCCTCCCA ATACGCTGGG ATTACAGGCG
TGAGCCACTG CGCCTGGCTG TTTGCTAACA TTTTAAAATT TCAACCTTCC TCTTCCTTAA
CTGGTCTTCC CCTACCCCCC
|
|
|
