|
|
| ID |
379 |
| OMIM_ID |
601859
|
| Disease |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME |
| Gene |
FAS
|
| SNP_ID |
rs2862833
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
10 |
| SNP
type |
Y |
| Length |
1000 |
| 5'
Near Seq 30 bp |
aagaagcat |
| 3'
Near Seq 30 bp |
aaagacaagttatatttagcatcagttaga |
| Fasta
Sequence |
CAGACAGCAC AGACTATGAT GGCTCAGAAA AGAGAAATTA ATGAGTGAAC CCTGTGATCA
CTCAGACTTT CTGCCTAAAG ACACTTTCCA GACCATAACA CAGGAGGGAA CCCTAAGCAA
AGCACAACTA TCTTACCGAC Atgcttacat gttgaaatgc taatactttg ggactcatgg
gttaaataga atatattact agcattaaat tGCAGAAAAG AAAGGTGGCC CACTGGCCAG
CATGTAGCTA GAATGGATAA TATGCAGGAA AGAATATTTC AAAATCCTCA TTTGGCTTTC
TTAATAATAA AACCTACCCC TTGAAATGTA TACTTTCTTA TCCACATTCC AGTATCTGGA
ATACGAAACT GTTTGACGAA TAATCATGTG CTGTTTGGAA GAGGTCTTCT TGGCAATAGC
AACCTATGGA AATAATTATT TAACTACTAA AAGGGTTAAG GTTAAAAAGG AAGTACCTTC
TAAGGGATCC AAGAAGCAT
Y
AAAGACAAGT TATATTTAGC ATCAGTTAGA GAAAAGGAAG ACAAAACCAA AAAGCAAGCC
CCTACCAAAA AAGAGAAAAC CAGAAATACC AAAAACATTA TTTAATTACG TACTTTTACC
TATATTTTAT AATTCCAAAC ACAAGGGGCA AAAAAATCCT CCATAAATGG AAGTTCTTTA
GGTGGTTCCA GGTATCTGCT TCAGTTTATA ACTATCTTCA CAGTTTACAT TTACAGAAAT
ATAAATATTA TTTCTTAAAA TTCACATTTA ATACAAACTT TCAAAGATAT TTAAACGTAG
GATAGTAGTA AGGAGAATCT TAAATCTTAG AAACTTGGGG GTATGACAAG AGCAATTCCT
AAATCCAGAT GATGATTTTA CCATTGCTAT GTATAAGCTG CCATTTGTAG CAGGTTTTAC
ATGGGACATT ATTGAACATT TTCGGGGGTG GGGGAAAAAT AAGAATCTAT TTTATCATCT
TTGATTGCAA ACATGGGTTC
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