|
|
| ID |
55 |
| OMIM_ID |
236100
|
| Disease |
HOLOPROSENCEPHALY |
| Gene |
SIX homeobox 3
|
| SNP_ID |
rs163538
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
R |
| Length |
609 |
| 5'
Near Seq 30 bp |
tcttgcctcccccatcggtgcccatggacc |
| 3'
Near Seq 30 bp |
cattcacctcaactccctcttcatcaatta |
| Fasta
Sequence |
ATCCCGGATT CCGAGGGTAT CTGGCGCCAG GGAGCCTGAG CCCAATTCCC AGGGTGCTGG
AGGCCGCTCT TGCCTCCCCC ATCGGTGCCC ATGGACC
R
CATTCACCTC AACTCCCTCT TCATCAATTA GGCTTCTCTT TACTCCCTCC CCGGCCAAGG
AGCCTCGATT TCCCCCACCA CCCTGTATTT TAAAATAACA GTCCAAACAG TACACTTCTT
TCCATCTTAA GAAGCAACTC AACTCTTTGT TTCTTCCCAG AATTCAGCTG CCTCTCTGAG
GAGTGGTGGA GGAGCTGCGG GAGCCGAGAA GCCCAAGAGC CCTCTGGACC CAGAAAAGTC
CTACAGATGC CCACTCCTCA CCACACAACA GAAGGAGCTC TGGTCCTGCC TGCCAGCCCC
AGAGGGCACT CAAACTTTGG AGGCCAGCCA CCCGGATGAA GTGAATAAGG CCTGAAAATT
GCTTGTTTGC TCGTATTGTA AAATAATAAT AATTACCATT ATTATTTTTA AACTGTCTAA
TTTCTCTAGG GAAAGTAACA TCGAAAGCCT AAAACAGACG CCAAAAGGCC CATAGAACAC
AGAGGGCCCT CTCTGCCTCT GGCCACCACA G
|
|
|
