|
|
| ID |
479 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17225067
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
R |
| Length |
511 |
| 5'
Near Seq 30 bp |
caaatattttggaagaaacaaatagctcag |
| 3'
Near Seq 30 bp |
gacctcgtaaaatatcttaaactggagggc |
| Fasta
Sequence |
ATAGTGTTAA CTGTCAGTGC CCATGGGCTA TCAACTTAAT AAGATATTTA GTAATATTTT
ACTTTGAGGA CATTTTCAAA GATTTTTATT TTGAAAAATG AGAGCTGTAA CTGAGGACTG
TTTGCAATTG ACATAGGCAA TAATAAGTGA TGTGCTGAAT TTTATAAATA AAATCATGTA
GTTTGTGGAA TTTGAGATGC ATTGTAGTTC TTCGCAGTGT GACTTCAAAT ATTTTGGAAG
AAACAAATAG CTCAG
R
GACCTCGTAA AATATCTTAA ACTGGAGGGC TCCATGGAGA TCATTGCGAG TGACTCCCCC
AGAATGTCCA TCTGTTGACA GGAGCCAGGC TGGCTGCATA CGAATTAGCT AAGGAGCTTA
TTATATATCC AGAGTCCTAC CGTGAGCCTC CATCCCGTCT GCCATTCTCC CATCCCTGGT
CTATGATAAG ACTTAGAAAT CTGGATTTTA ACAAAACGTT TCAGATTGAG AACCTTGATT
TAGTCTACTT CTCCT
|
|
|
