|
|
| ID |
53 |
| OMIM_ID |
236100
|
| Disease |
HOLOPROSENCEPHALY |
| Gene |
SIX homeobox 3
|
| SNP_ID |
rs741813
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/T
|
| Orientation |
fwd/B |
| Chr-Number |
2 |
| SNP
type |
W |
| Length |
816 |
| 5'
Near Seq 30 bp |
gagccctctggacccagaaaagtcctacag |
| 3'
Near Seq 30 bp |
tgcccactcctcaccacacaacagaaggag |
| Fasta
Sequence |
TGCCTCTCTG AGGAGTGGTG GAGGAGCTGC GGGAGCCGAG AAGCCCAAGA GCCCTCTGGA
CCCAGAAAAG TCCTACAG
W
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 AGTGTGATTT ACGCAGATTT GTCGGGGTCA GAGACGTCTT TCCCTGAGCA
CTGTGTATAT TTAGACAGGA CTCGGTTTGG TGTTAAAAAG TGTATATGTT GAATGGATTC
ACACACAGTA GCCAACAATG ACCACATTGT CGGCCCGTGT ACAACGCGTA TTGAAACGCA
GCGCCCAGAC TTCAACTAAT CTGCCCTCAA TAAAGCTGAA ATAATTATCC TAAGCTGCCT
TTCCAGAAGA AAAATCATTG AGGAATTCAA AACTTTTTTT TTTTTTTTTT AAAGATCTTT
TCTGCATTCC GAAGCAAATC TGGGGGCAAG GCGCCGGTCC ACACCACTTT GGTGATCTCA
ATGAGGGAAA AAGAAAA
|
|
|
