|
|
| ID |
461 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17224066
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/C
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
M |
| Length |
511 |
| 5'
Near Seq 30 bp |
cgccatgttggccaggctggtctcaaactc |
| 3'
Near Seq 30 bp |
ggacctcaggtgatccacccgcgttggcct |
| Fasta
Sequence |
TGGATCCTGA GCTCCTTCAG GTGTTTGATA ACATTTTATT TATTTTTTGA GACAGAGTCT
CGCTCTGTCA CCGAGGCTGG AGTGTAGTGG CGCGATCTTG GCTCACTGCC CCCTCCACCT
CCCAGGTTCA AGAGATTCTC CTGCCTCAGC CTCTCGAGTA GCTGTGATTA CAGGCGCCCA
CCACTATGCC CGGTAATTTT TGTATTTTTA GTAGAGACGG GGTTTCGCCA TGTTGGCCAG
GCTGGTCTCA AACTC
M
GGACCTCAGG TGATCCACCC GCGTTGGCCT CCCAATACGC TGGGATTACA GGCGTGAGCC
ACTGCGCCTG GCTGTTTGCT AACATTTTAA AATTTCAACC TTCCTCTTCC TTAACTGGTC
TTCCCCTACC CCCCCTCAAG ACGGGGTCTC TCGCTCTGTC GCCCCAGCTG CGGTGCAGTG
GCGTGAACAT AGCTGACGGC AGAAGACCTC CTGGGCTCAA ACGATCCTCC TGGCTCGTGC
TCCCAAAGTA CTGGG
|
|
|
