|
|
| ID |
472 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17224080
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
G/T
|
| Orientation |
fwd/B |
| Chr-Number |
2 |
| SNP
type |
K |
| Length |
511 |
| 5'
Near Seq 30 bp |
atagcaggccatataaatgttttcgaatga |
| 3'
Near Seq 30 bp |
tgaatcatcaacgagtggatgaaacgataa |
| Fasta
Sequence |
GTCAATCTCC TGGGCTCAAG TGATCCGCCC ACCTCGGCCT CCCAAATTGC TGGGATTACA
GGCGTGAGCT ACCGCGCCCT GCCACAAACG CATATCTTCT AACGTACCAT TTCATTTACT
TGCTATATTC ATTATCTGAA TCTTCTCATA TTAGAATGTA AGCAGAATAA AGGCAGTGAT
TTTTCTTTTT ACTGGCGATC CTCAGAGCCA AGAAGAGTCT GGGACATAGC AGGCCATATA
AATGTTTTCG AATGA
K
TGAATCATCA ACGAGTGGAT GAAACGATAA TGTGGCTAAC AGGCAGCAGT AAGGAGGCTG
TGTAGAATAA ACCCGTAATC CCGATGTTGG CAGTTTGCTT AGAAAGAAAA AGGGAGGCAG
TCGGAGAGGG GCACACGTTT TAACAAAATA CTGGGAGGAG GAGGAAGGCT AGTTTTTTTT
TTGTTTTCAA GTTTCCTTCT GATGTTACTC CCATGCTTCC GGGCACATTA CGAGCTCAGT
GCCTGCCGGA AATCT
|
|
|
