|
|
| ID |
111 |
| OMIM_ID |
160900
|
| Disease |
DYSTROPHIA MYOTONICA |
| Gene |
DMPK
|
| SNP_ID |
rs34321594
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/AAG
|
| Orientation |
fwd/ |
| Chr-Number |
19 |
| SNP
type |
N |
| Length |
601 |
| 5'
Near Seq 30 bp |
acagaggaagccacaggtgtgatgaatttc |
| 3'
Near Seq 30 bp |
aagaacctgcccattgctgaaacagggcca |
| Fasta
Sequence |
CAGGCCCTGG AGCCCTGGCT GCATGTCTGC CTGTCCCTGG CTGTCCCCTG GGCCTCTCTG
GCCACTTCTC TCTGCGGCCG GCCGAGGCCT CCTCCCCTTC TCCCCACCCC TTGGTCCAGC
CCCCCTCCCG CCTCCCAGCC TTAACCCCTC ACAAGCCAGC CCCCCAAGCT CCCTCCTTCC
AGGGCCCTTC AGAACCCTTC AGTGCTAGAG TAGGGGGAAT GCATGGAGAA TCTCAGCTGT
CACACTGTCA CCCCAATAAA AAGGTAGAGC ACAGAGGAAG CCACAGGTGT GATGAATTTC
N
AAGAACCTGC CCATTGCTGA AACAGGGCCA ATTGAGGCTG AGTGACCCAG TAGCAACCAC
CCCCTTGCTC CCGACAAGCT CCAGAACTGG GGGCTAGGGG GTGAGGGCTG GGGGTTGGGG
CTGGGTGGGA GAAAGGGGTT GAGGCCTGGG AAGGGGACGG GAGGCCAGGG CAGCTTCTTG
GGTGACTCAG AGATGGATTC CGACTCGGAC AGTTAAATTT AGCCCTCAGG CTCTCTGCTT
TATACCAGCT TTTTTTTTTT TTTTTTTTTT TTTCCCAGGA GGTGGGGAAG GGGTGGTGAG
|
|
|
