|
|
| ID |
481 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs17218676
|
| 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 |
cttctcctattttacaataaagagatgaag |
| 3'
Near Seq 30 bp |
ggttaagaattagctaatcctacgcaaagt |
| Fasta
Sequence |
TGGAGGGCTC CATGGAGATC ATTGCGAGTG ACTCCCCCAG AATGTCCATC TGTTGACAGG
AGCCAGGCTG GCTGCATACG AATTAGCTAA GGAGCTTATT ATATATCCAG AGTCCTACCG
TGAGCCTCCA TCCCGTCTGC CATTCTCCCA TCCCTGGTCT ATGATAAGAC TTAGAAATCT
GGATTTTAAC AAAACGTTTC AGATTGAGAA CCTTGATTTA GTCTACTTCT CCTATTTTAC
AATAAAGAGA TGAAG
Y
GGTTAAGAAT TAGCTAATCC TACGCAAAGT GAGGGAAAAA GGACAGTCTT TTTAATAAAT
GCGGCGGGCT GGTGGGGTAT CCATATAGGA AGAAATGACA TTGGACCCCT ACTCCATGTC
ATATATAAAA ACCTCCACTT TGGGAGGCGA AGCAGGCAAT CACTTGAACT CAGGAGATCA
AGACCAGCCT GGACAACATG ACGAAACCCC ATCTCTACAA AAATAAATGC AAAAATTAGC
CGGGCATAGT GGTGC
|
|
|
