|
|
| ID |
SNP10.028 |
| OMIM_ID |
137750
|
| Disease |
GLAUCOMA |
| Gene |
MYOC(myocilin)
|
| SNP_ID |
rs59892130
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
chromosome 1 |
| SNP
type |
R |
| Length |
601 |
| 5'
Near Seq 30 bp |
tcagaaaaagccatctcaagaatttgtctg |
| 3'
Near Seq 30 bp |
tgacttaaaagcagaggttctcagattgga |
| Fasta
Sequence |
>gnl|dbSNP|rs59892130|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=129
CCACCCCTTT TTTCTTTCTT CCTTGGCACT GACATCTTTG ACCAGTCCAA ACTAATTGTC
CAACAACTGG ATTTGCTTGC TTATTTCCTC ATGATTAGAA CACTTCCTCA ACAGGGAATA
TTTGGGAGCC CACTTTCACA AAAAGTGACA CAAATACCAT CTTCCCAGCT AATAAGAAGA
CCTCCCCCAA CACCTCACCC CCGCACCCCC CCCACACACA CACAGACTCA CCTTTAGGCA
AGAAGGGACC AGGATGAACA GAAGAGCCTC TCAGAAAAAG CCATCTCAAG AATTTGTCTG
R
TGACTTAAAA GCAGAGGTTC TCAGATTGGA CTGAGTAAGA AAACTTTCAG AACAACATAT
TAAGAAAACT GACAGAGAGG TGCCATCTCT TTATTTTGCC AGGGAAGAAC ATTTAAAAAT
AAACAAAAAC TTACCACTTA TTATCATTTC CCAAATCTAT TGTAATTTCA TAAATAAAGG
TCATTTTAAC ATCAAAAGGT ACAAATAACA ATCTGAGCAA AGGTTCAAAA AAGGATAGTT
TTTCAAAAGG GACAATTGAC AACTTTCTAC TGCTCATATG CAGACACATC TCACCCGGTC
|
|
|
