|
|
| ID |
109 |
| OMIM_ID |
160900
|
| Disease |
DYSTROPHIA MYOTONICA |
| Gene |
DMPK
|
| SNP_ID |
rs35008423
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/C
|
| Orientation |
fwd/ |
| Chr-Number |
19 |
| SNP
type |
N |
| Length |
601 |
| 5'
Near Seq 30 bp |
cacacgcctccggattggcccgctgcggag |
| 3'
Near Seq 30 bp |
ctccggcccacaacgcaaaccgcggacact |
| Fasta
Sequence |
TTTCTCGAGC TTGCGTCCCA GGAGCGGATG CGCGTGGCGT GCGCAGGCGC AGTGGAAGGA
GGATGGCCGC GCGCGCTGCC AGCCCAGCCC CCTCTTCTCG ACGCTCGGTG GCACAGCTGG
GCCACAGCTG GGCGGGGGCG GTGCCTCCGG GTGGCCCGCT CGCCCTCCTA TTGGCCGGAC
GCCAAAGCCC CGCCCCGTGG CTTTTCCTCC CCCAACCCTG ATTCGGCCGC TTCGCATCCC
GCTAGCTCCT CCCAGACCTT CGGCCGCCTC CACACGCCTC CGGATTGGCC CGCTGCGGAG
N
CTCCGGCCCA CAACGCAAAC CGCGGACACT GTGGAGTCCA GAGCTTTGGG CAGATGGAGG
GCCTTTTATT CGCGAGGGTC GGGGGTGGGG GTCCTAGGTG GGGACAGACA ATAAATACCG
AGGAATGTCG GGGTCTCAGT GCATCCAAAA CGTGGATTGG GGTTGTTGGG GGTCCTGTAG
CCTGTCAGCG AGTCGGAGGA CGAGGTCAAT AAATATCCAA ACCGCCGAAG CGGGCGGAGC
CGGCTGGGGC TCCGAGAGCA GCGCAAGTGA GGAGGGGGGC GCGGGATCCC CGAAAAAGCG
|
|
|
