|
|
| ID |
480 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17218669
|
| 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 |
gcctccatcccgtctgccattctcccatcc |
| 3'
Near Seq 30 bp |
tggtctatgataagacttagaaatctggat |
| Fasta
Sequence |
TGTAGTTTGT GGAATTTGAG ATGCATTGTA GTTCTTCGCA GTGTGACTTC AAATATTTTG
GAAGAAACAA ATAGCTCAGA GACCTCGTAA AATATCTTAA ACTGGAGGGC TCCATGGAGA
TCATTGCGAG TGACTCCCCC AGAATGTCCA TCTGTTGACA GGAGCCAGGC TGGCTGCATA
CGAATTAGCT AAGGAGCTTA TTATATATCC AGAGTCCTAC CGTGAGCCTC CATCCCGTCT
GCCATTCTCC CATCC
M
TGGTCTATGA TAAGACTTAG AAATCTGGAT TTTAACAAAA CGTTTCAGAT TGAGAACCTT
GATTTAGTCT ACTTCTCCTA TTTTACAATA AAGAGATGAA GCGGTTAAGA ATTAGCTAAT
CCTACGCAAA GTGAGGGAAA AAGGACAGTC TTTTTAATAA ATGCGGCGGG CTGGTGGGGT
ATCCATATAG GAAGAAATGA CATTGGACCC CTACTCCATG TCATATATAA AAACCTCCAC
TTTGGGAGGC GAAGC
|
|
|
