|
|
| ID |
474 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17224094
|
| 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 |
caccagcgtgcgcgggaagctgggccgcgt |
| 3'
Near Seq 30 bp |
tgcttatgattggttgccgcggcagactcc |
| Fasta
Sequence |
TTTTGTTTTC AAGTTTCCTT CTGATGTTAC TCCCATGCTT CCGGGCACAT TACGAGCTCA
GTGCCTGCCG GAAATCTCCC ACCTGGTGGC AACCTACCCT TGCATACACC CCACCCAGGG
GCTTCAAGCC TTGCAGCTGA GTAAACACAG AAAGGAGCTC TACTAAGGAT GCGCGTCTGC
GGGTTTCCGC GCGACCTAGG CGCAGGCATG CGCAGTAGCT AAAGTCACCA GCGTGCGCGG
GAAGCTGGGC CGCGT
Y
TGCTTATGAT TGGTTGCCGC GGCAGACTCC CACCCACCGA AACGCAGCCC TGGAAGCTGA
TTGGGTGTGG TCGCCGTGGC CGGACGCCGC TCGGGGGACG TGGGAGGGGA GGCGGGAAAC
AGCTTAGTGG GTGTGGGGTC GCGCATTTTC TTCAACCAGG AGGTGAGGAG GTTTCGACAT
GGCGGTGCAG CCGAAGGAGA CGCTGCAGTT GGAGAGCGCG GCCGAGGTCG GCTTCGTGCG
CTTCTTTCAG GGCAT
|
|
|
