|
|
| ID |
410 |
| OMIM_ID |
118200
|
| Disease |
CHARCOT-MARIE-TOOTH DISEASE |
| Gene |
MPZ
|
| SNP_ID |
rs10530996
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/CT
|
| Orientation |
fwd/T |
| Chr-Number |
1 |
| SNP
type |
N |
| Length |
801 |
| 5'
Near Seq 30 bp |
atctcataagtagcataatatttcatttga |
| 3'
Near Seq 30 bp |
ctctctctctctctttcttttttattttta |
| Fasta
Sequence |
CGATTTATTT CAAAGTAATA ATTAGATGGG ATTCAAAGTT TCCCATATAA CAATGTCATT
TCCCTTTATC TGAATCATTA TTCTAGACTT TATTTAATGC TTTACTGCAG AGGAAAGAAA
GGGGGGATGT GGCTTACTTT GTTGGGGATT GTGGAAAATG GGCACAGTCC TGGAAAAACC
CACATTAAGT GTGCAATGCT TGTGAAAATG CCTAATGCAA GAGATTGCAA AATGTTGTCC
CAGGGTACCA GGATTCTTGA TGGAATAAGA AATATTAAAA TAATTGGATA AACTGAGCTA
GCAAAATGCA GGTGGCTGAT AAATTTTAGA ACAAAAGTGT AATTAAATGA GAAGCTTTGA
GCTATACTCT ATCTCATAAG TAGCATAATA TTTCATTTGA
N
CTCTCTCTCT CTCtttcttt tttattttta tgagacatag tctcgctgtg ttgcccaggc
tagagtgcag cggcatgatc tcggctcact gcaacctccg cctccgcggt tcaagcaatt
ctcgtgcccc agctgcccaa gtagccaggg ttagaaggcg ttcaccacca tgctcggcta
atttttgtat ttttagtgga gacagtgttt agccatgttg gtcaggctgg cctcaacctc
ctagcctgaa gtgatctgcc cacctcggcc tcccaaagtg ctggcattac aggcatgagc
caccacatcc aaccTCATTT GACTCTCCTG ACAGTCTGGG AAGTTTAAGC AGGGAACCCA
GCTGCAACTA TCTAATGAAT AATGGACAGT TTAGCATCTT
|
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