|
|
| ID |
482 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17218683
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/B |
| Chr-Number |
2 |
| SNP
type |
S |
| Length |
511 |
| 5'
Near Seq 30 bp |
atccatataggaagaaatgacattggaccc |
| 3'
Near Seq 30 bp |
tactccatgtcatatataaaaacctccact |
| Fasta
Sequence |
GAGTCCTACC GTGAGCCTCC ATCCCGTCTG CCATTCTCCC ATCCCTGGTC TATGATAAGA
CTTAGAAATC TGGATTTTAA CAAAACGTTT CAGATTGAGA ACCTTGATTT AGTCTACTTC
TCCTATTTTA CAATAAAGAG ATGAAGCGGT TAAGAATTAG CTAATCCTAC GCAAAGTGAG
GGAAAAAGGA CAGTCTTTTT AATAAATGCG GCGGGCTGGT GGGGTATCCA TATAGGAAGA
AATGACATTG GACCC
S
TACTCCATGT CATATATAAA AACCTCCACT TTGGGAGGCG AAGCAGGCAA TCACTTGAAC
TCAGGAGATC AAGACCAGCC TGGACAACAT GACGAAACCC CATCTCTACA AAAATAAATG
CAAAAATTAG CCGGGCATAG TGGTGCTTGC CTGTAGTCCC AGCTACTCAG GAGGCTGAGG
TGGGAGGATC ACGTGATCTG GGAGAGGTTG AGGTTACAGT GAGCTGCACT CCATCCTGGG
TAATACAGTG ATAAC
|
|
|
