|
|
| ID |
462 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17224073
|
| 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 |
acgtttgtctttttatttattttattttgt |
| 3'
Near Seq 30 bp |
ttttttgagacagggttttcaatctgtcgc |
| Fasta
Sequence |
TGCGCCTGGC TGTTTGCTAA CATTTTAAAA TTTCAACCTT CCTCTTCCTT AACTGGTCTT
CCCCTACCCC CCCTCAAGAC GGGGTCTCTC GCTCTGTCGC CCCAGCTGCG GTGCAGTGGC
GTGAACATAG CTGACGGCAG AAGACCTCCT GGGCTCAAAC GATCCTCCTG GCTCGTGCTC
CCAAAGTACT GGGATTATGG CGTGTGACAC CACGCCTGGC GTCAAACGTT TGTCTTTTTA
TTTATTTTAT TTTGT
R
TTTTTTGAGA CAGGGTTTTC AATCTGTCGC CCACGCTGGA GTGCAGTGGC ACAATTTACG
GCTCACCGCA GCCTCGACCT CCCGGGCTCA GGTGATCCTT TCGCCTCAGC CCTGCTAATA
TCTGGGATCA CAGACGTGGG TTTTACCATG TTGCCCAGGA TGGTGTCAAT CTCCTGGGCT
CAAGTGATCC GCCCACCTCG GCCTCCCAAA TTGCTGGGAT TACAGGCGTG AGCTACCGCG
CCCTGCCACA AACGC
|
|
|
