|
|
| ID |
54 |
| OMIM_ID |
236100
|
| Disease |
HOLOPROSENCEPHALY |
| Gene |
SIX homeobox 3
|
| SNP_ID |
rs1561226
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
R |
| Length |
713 |
| 5'
Near Seq 30 bp |
accgcattcacctcaactccctcttcatca |
| 3'
Near Seq 30 bp |
ttaggcttctctttactccctccccggcca |
| Fasta
Sequence |
CCCGGATTCC GAGGGTATCT GGCGCCAGGG AGCCTGAGCC CAATTCCCAG GGTGCTGGAG
GCCGCTCTTG CCTCCCCCAT CGGTGCCCAT GGACCGCATT CACCTCAACT CCCTCTTCAT
CA
R
TTAGGCTTCT CTTTACTCCC TCCCCGGCCA AGGAGCCTCG ATTTCCCCCA CCACCCTGTA
TTTTAAAATA ACAGTCCAAA CAGTACACTT CTTTCCATCT TAAGAAGCAA CTCAACTCTT
TGTTTCTTCC CAGAATTCAG CTGCCTCTCT GAGGAGTGGT GGAGGAGCTG CGGGAGCCGA
GAAGCCCAAG AGCCCTCTGG ACCCAGAAAA GTCCTACAGA TGCCCACTCC TCACCACACA
ACAGAAGGAG CTCTGGTCCT GCCTGCCAGC CCCAGAGGGC ACTCAAACTT TGGAGGCCAG
CCACCCGGAT GAAGTGAATA AGGCCTGAAA ATTGCTTGTT TGCTCGTATT GTAAAATAAT
AATAATTACC ATTATTATTT TTAAACTGTC TAATTTCTCT AGGGAAAGTA ACATCGAAAG
CCTAAAACAG ACGCCAAAAG GCCCATAGAA CACAGAGGGC CCTCTCTGCC TCTGGCCACC
ACAGCCCCTA GGCCAGGCAT GGGTATTTAT TCTTAGGTAT GTTGCTTTTA AGAAGCTGTA
ATCAGCATCT TGAGCCGGGC CTCCCTTTGT GAGGCTTCTG TAACTATGGA
|
|
|
