|
|
| ID |
SNP10.049 |
| OMIM_ID |
137750
|
| Disease |
GLAUCOMA |
| Gene |
MYOC(myocilin)
|
| SNP_ID |
rs58117216
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 1 |
| SNP
type |
Y |
| Length |
601 |
| 5'
Near Seq 30 bp |
gaacacagcactagacatgaataaagacca |
| 3'
Near Seq 30 bp |
gtgggcacaaaagggaagaaacttaacttc |
| Fasta
Sequence |
>gnl|dbSNP|rs58117216|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129
GTAACTTCTC AAGTATATCT AATTCTACAT GACAATCAAG TGGATGAAAT CAACACATCT
CTCATCTTGC CCTGTGCAGC CCAGCCCAGC CTCCCAAGTG TGGGTGATAG GATAGAGGGC
TTTGTTAGGG AAAGGCTGAC TCCTGCAGAC CTGCTCTGAC AAGGGAACAG AGAGAGAGAG
AGAGTTCTGT TCCTCTTCTC CTCCCCTCCC TCTGCTCCCA GGGAAGTTAA TTTCCCCCTT
GGGTGGGCAT TTACCCTATA CTGATTCTCT GAACACAGCA CTAGACATGA ATAAAGACCA
Y
GTGGGCACAA AAGGGAAGAA ACTTAACTTC ATACCGGTGT CTCCCTCTCC ACTCCTGAGA
TAGCCAGATG GGCTCTCCTT CAAAATTCGG GAAGCAGGAA CTTCAGTTAG CTCGGACTTC
AGTTCCTGGA AGGCCAAAGT GTCCAAATTC CACGTAGAAA CTGCATTAAA AGAAAGAGAC
AAAATTTTAC TGTAAGAAAA AATGGCCCAA GGATTGACTA TGTTGAGGAT GACATTTAAA
TAGGCTGCCG GCCAGGCGTG GTGGCTCATG CCTGTAATCC CAGCACTTTG GGAGGCCGAG
|
|
|
