|
|
| ID |
470 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs756562
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
2 |
| SNP
type |
Y |
| Length |
589 |
| 5'
Near Seq 30 bp |
tgctatattcattatctgaatcttctcata |
| 3'
Near Seq 30 bp |
tagaatgtaagcagaataaaggcagtgatt |
| Fasta
Sequence |
ttttaccatg ttgcccagga tggtgtcaat ctcctgggct caagtgatcc gcccacctcg
gcctcccaaa ttgctgggat tacaggcgtg agctaccgcg ccctgccACA AACGCATATC
Ttctaacgta ccatttcatt tacttgctat attcattatc tgaatcttct cata
Y
tagaatgtaa gcagaataaa ggcagtgatt tttcttttta ctggcgatcc tcagagccaa
gaagagtctg ggacatagca ggccatataa atgttttcga atgagtgaat CATCAACGAG
TGGATGAAAC GATAATGTGG CTAACAGGCA GCAGTAAGGA GGCTGTGTAG AATAAACCCG
TAATCCCGAT GTTGGCAGTT TGCTTAGAAA GAAAAAGGGA GGCAGTCGGA GAGGGGCACA
CGTTTTAACA AAATACTGGG AGGAGGAGGA AGGCTAGTTT TTTTTTGTTT TCAAGTTTCC
TTCTGATGTT ACTCCCATGC TTCCGGGCAC ATTACGAGCT CAGTGCCTGC CGGAAATCTC
CCACCTGGTG GCAACCTACC CTTGCATACA CCCCACCCAG GGGCTTCAAG CCTT
|
|
|
