|
|
| ID |
475 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17224101
|
| 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 |
gctgggccgcgtctgcttatgattggttgc |
| 3'
Near Seq 30 bp |
gcggcagactcccacccaccgaaacgcagc |
| Fasta
Sequence |
TTCTGATGTT ACTCCCATGC TTCCGGGCAC ATTACGAGCT CAGTGCCTGC CGGAAATCTC
CCACCTGGTG GCAACCTACC CTTGCATACA CCCCACCCAG GGGCTTCAAG CCTTGCAGCT
GAGTAAACAC AGAAAGGAGC TCTACTAAGG ATGCGCGTCT GCGGGTTTCC GCGCGACCTA
GGCGCAGGCA TGCGCAGTAG CTAAAGTCAC CAGCGTGCGC GGGAAGCTGG GCCGCGTCTG
CTTATGATTG GTTGC
Y
GCGGCAGACT CCCACCCACC GAAACGCAGC CCTGGAAGCT GATTGGGTGT GGTCGCCGTG
GCCGGACGCC GCTCGGGGGA CGTGGGAGGG GAGGCGGGAA ACAGCTTAGT GGGTGTGGGG
TCGCGCATTT TCTTCAACCA GGAGGTGAGG AGGTTTCGAC ATGGCGGTGC AGCCGAAGGA
GACGCTGCAG TTGGAGAGCG CGGCCGAGGT CGGCTTCGTG CGCTTCTTTC AGGGCATGCC
GGAGAAGCCG ACCAC
|
|
|
