|
|
| ID |
468 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17217681
|
| 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 |
gccacaaacgcatatcttctaacgtaccat |
| 3'
Near Seq 30 bp |
tcatttacttgctatattcattatctgaat |
| Fasta
Sequence |
CAATCTGTCG CCCACGCTGG AGTGCAGTGG CACAATTTAC GGCTCACCGC AGCCTCGACC
TCCCGGGCTC AGGTGATCCT TTCGCCTCAG CCCTGCTAAT ATCTGGGATC ACAGACGTGG
GTTTTACCAT GTTGCCCAGG ATGGTGTCAA TCTCCTGGGC TCAAGTGATC CGCCCACCTC
GGCCTCCCAA ATTGCTGGGA TTACAGGCGT GAGCTACCGC GCCCTGCCAC AAACGCATAT
CTTCTAACGT ACCAT
Y
TCATTTACTT GCTATATTCA TTATCTGAAT CTTCTCATAT TAGAATGTAA GCAGAATAAA
GGCAGTGATT TTTCTTTTTA CTGGCGATCC TCAGAGCCAA GAAGAGTCTG GGACATAGCA
GGCCATATAA ATGTTTTCGA ATGAGTGAAT CATCAACGAG TGGATGAAAC GATAATGTGG
CTAACAGGCA GCAGTAAGGA GGCTGTGTAG AATAAACCCG TAATCCCGAT GTTGGCAGTT
TGCTTAGAAA GAAAA
|
|
|
