|
|
| ID |
SNP11.52 |
| OMIM_ID |
300400
|
| Disease |
Severe combined immunodeficiency |
| Gene |
IL2RG
|
| SNP_ID |
rs5981074
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome X |
| SNP
type |
Y |
| Length |
801 |
| 5'
Near Seq 30 bp |
ttacaggcgtgagccaccacgcccagccca |
| 3'
Near Seq 30 bp |
tgtaagtctaactctaaactaaaccctgga |
| Fasta
Sequence |
>gnl|dbSNP|rs5981074|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=126
GTGGCCAAAA AGTGGAGTAA GGGTAAGGAG AGAAAAACTT GGGTGGGGTA TGTTAAAGAT
TAGTTGGAAA GGGGGGACAA CATGGTAAGT CTAACttttt ttattttttt tattttttta
gatggagtct ccctctgtcg cccaggctgg agtgcagtgg cacaatcttg gctcactgca
tcctctacct cctgggttca agcgattctc ctgcctcagc ctcccaagta gctggaatta
caggagcaca ccatcacgcc tggctaattt ttgtattttt agtagagacg gggtttcacc
atgttggcca ggctggtctc gatctcctga cctcgtgatc cacccgcttt ggcctcccaa
agtgctggga ttacaggcgt gagccaccac gcccagccCA
Y
TGTAAGTCTA ACTCTAAACT AAACCCTGGA ATGAGTGCAG GGCACCTGGA AAAAAGTCAG
TTTCCAGAAC AGTACTCTTT CTAGCAAATT GGTAATACTC CTGCCTCCAC AGCATGAATG
TACTACTCCT TTTTCTTCCC CTCCCACCCT CATTGCATCC CAGGCTTCCC CTGCTCCCCA
CCCCCATGAC AGACATTTTT GATGATTATC AACAGAAACT TTATTTCTCA TCGGTTCAGG
AACAATCGGA GGGTAGATgg aaagaggaag ggagggaaag agggagggag gaagAATCCT
GCGAAAAGGA AGGGCCAGAC TGAGGGAGAA GAAAAACATG TTCGGGGCAA AAGGGTAATT
CTCAAGTGGG GAATGCCAAA TGAAGGGGTG CTTACATGGG
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