|
|
| ID |
473 |
| OMIM_ID |
120435
|
| Disease |
LYNCH SYNDROME |
| Gene |
MSH2
|
| SNP_ID |
rs1863332
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/C
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
M |
| Length |
670 |
| 5'
Near Seq 30 bp |
gagtaacatcagaaggaaacttgaaaacaa |
| 3'
Near Seq 30 bp |
aaaaaaactagccttcctcctcctcccagt |
| Fasta
Sequence |
CTCCGGCATG CCCTGAAAGA GCGCACGAAG CCGACCTCGG CCGCGCTCTC CAACTGCAGC
GTCTCCTTCG GCTGCACCGC CATGTCGAAA CCTCCTCACC TCCTGGTTGA AGAAAATGCG
CGACCCCACA CCCACTAAGC TGTTTCCCGC CTCCCCTCCC ACGTCCCCCG AGCGGCGTCC
GGCCACGGCG ACCACACCCA RTCAGCTTCC AGGGCTGCGT TTCGGTGGGT GGGAGTCTGC
CGCGGCAACC AATCATAAGC AGACGCGGCC CAGCTTCCCG CGCACGCTGG TGACTTTAGC
TACTGCGCAT GCCTGCGCCT AGGTCGCGCG GAAACCCGCA GACGCGCATC CTTAGTAGAG
CTCCTTTCTG TGTTTACTCA GCTGCAAGGC TTGAAGCCCC TGGGTGGGGT GTATGCAAGG
GTAGGTTGCC ACCAGGTGGG AGATTTCCGG CAGGCACTGA GCTCGTAATG TGCCCGGAAG
CATGGGAGTA ACATCAGAAG GAAACTTGAA AACAA
M
AAAAAAACTA GCCTTCCTCC TCCTCCCAGT ATTTTGTTAA AACGTGTGCC CCTCTCCGAC
TGCCTCCCTT TTTCTTTCTA AGCAAACTGC CAACATCGGG ATTACGGGTT TATTCTACAC
AGCCTCCTTA CTGCTGCCTG TTAGCCACAT TATC
|
|
|
