|
|
| ID |
48 |
| OMIM_ID |
236100
|
| Disease |
HOLOPROSENCEPHALY |
| Gene |
SIX homeobox 3
|
| SNP_ID |
rs83995
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/C
|
| Orientation |
fwd/T |
| Chr-Number |
2 |
| SNP
type |
M |
| Length |
816 |
| 5'
Near Seq 30 bp |
tttattcttaggtatgttgcttttaagaag |
| 3'
Near Seq 30 bp |
tgtaatcagcatcttgagccgggcctccct |
| Fasta
Sequence |
TGCCTCTCTG AGGAGTGGTG GAGGAGCTGC GGGAGCCGAG AAGCCCAAGA GCCCTCTGGA
CCCAGAAAAG TCCTACAGTT GCCCACTCCT CACCACACAA CAGAAGGAGC TCTGGTCCTG
CCTGCCAGCC CCAGAGGGCA CTCAAACTTT GGAGGCCAGC CACCCGGATG AAGTGAATAA
GGCCTGAAAA TTGCTTGTTT GCTCGTATTG TAAAATAATA ATAATTACCA TTATTATTTT
TAAACTGTCT AATTTCTCTA GGGAAAGTAA CATCGAAAGC CTAAAACAGA CGCCAAAAGG
CCCATAGAAC ACAGAGGGCC CTCTCTGCCT CTGGCCACCA CAGCCCCTAG GCCAGGCATG
GGTATTTATT CTTAGGTATG TTGCTTTTAA GAAG
M
TGTAATCAGC ATCTTGAGCC GGGCCTCCCT TTGTGAGGCT TCTGTAACTA TGGAAGTGTG
ATTTACGCAG ATTTGTCGGG GTCAGAGACG TCTTTCCCTG AGCACTGTGT ATATTTAGAC
AGGACTCGGT TTGGTGTTAA AAAGTGTATA TGTTGAATGG ATTCACACAC AGTAGCCAAC
AATGACCACA TTGTCGGCCC GTGTACAACG CGTATTGAAA CGCAGCGCCC AGACTTCAAC
TAATCTGCCC TCAATAAAGC TGAAATAATT ATCCTAAGCT GCCTTTCCAG AAGAAAAATC
ATTGAGGAAT TCAAAACTTT TTTTTTTTTT TTTTAAAGAT CTTTTCTGCA TTCCGAAGCA
AATCTGGGGG CAAGGCGCCG GTCCACACCA CTTTGGTGAT CTCAATGAGG GAAAAAGAAA
A
|
|
|
