|
|
| ID |
476 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs2303425
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
2 |
| SNP
type |
Y |
| Length |
670 |
| 5'
Near Seq 30 bp |
cacccaccgaaacgcagccctggaagctga |
| 3'
Near Seq 30 bp |
tgggtgtggtcgccgtggccggacgccgct |
| Fasta
Sequence |
GATAATGTGG CTAACAGGCA GCAGTAAGGA GGCTGTGTAG AATAAACCCG TAATCCCGAT
GTTGGCAGTT TGCTTAGAAA GAAAAAGGGA GGCAGTCGGA GAGGGGCACA CGTTTTAACA
AAATACTGGG AGGAGGAGGA AGGCTAGTTT TTTTKTTGTT TTCAAGTTTC CTTCTGATGT
TACTCCCATG CTTCCGGGCA CATTACGAGC TCAGTGCCTG CCGGAAATCT CCCACCTGGT
GGCAACCTAC CCTTGCATAC ACCCCACCCA GGGGCTTCAA GCCTTGCAGC TGAGTAAACA
CAGAAAGGAG CTCTACTAAG GATGCGCGTC TGCGGGTTTC CGCGCGACCT AGGCGCAGGC
ATGCGCAGTA GCTAAAGTCA CCAGCGTGCG CGGGAAGCTG GGCCGCGTCT GCTTATGATT
GGTTGCCGCG GCAGACTCCC ACCCACCGAA ACGCAGCCCT GGAAGCTGA
Y
TGGGTGTGGT CGCCGTGGCC GGACGCCGCT CGGGGGACGT GGGAGGGGAG GCGGGAAACA
GCTTAGTGGG TGTGGGGTCG CGCATTTTCT TCAACCAGGA GGTGAGGAGG TTTCGACATG
GCGGTGCAGC CGAAGGAGAC GCTGCAGTTG GAGAGCGCGG CCGAGGTCGG CTTCGTGCGC
TCTTTCAGGG CATGCCGGAG
|
|
|
