|
|
| ID |
SNP11.36 |
| OMIM_ID |
300400
|
| Disease |
Severe combined immunodeficiency |
| Gene |
IL2RG
|
| SNP_ID |
rs10609482
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/AAA
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome X |
| SNP
type |
N |
| Length |
801 |
| 5'
Near Seq 30 bp |
acaacaagagcgaaactctgtcccaaaaaa |
| 3'
Near Seq 30 bp |
aaaaaaaaaacctaccttgagctggtggat |
| Fasta
Sequence |
>gnl|dbSNP|rs10609482|allelePos=401|totalLen=801|taxid=9606|snpclass=2|alleles='-/AAA'|mol=Genomic|build=119
ggcagaggtt gcagtgagcc aagatcatgc cactgtttca gcctgggtga cagagcaaga
ctccatcaca aaaaataaaa taaataaata aataaaaaTA AAGACTACCT Tgccgggcac
agtggctcac gcctgtaatc ccagcacttt gggaggctga ggtgggtgga tcacctgagg
tcaggagttc aagaccagct tggccaacat ggtgaaaccc catctgcact aaaaaattag
ttgggcctgg tggcgggtgc ctgtagtccc agctactcag gaggctaaga caggagaatc
gcttgaacct gggaggcaga ggttgcagtg agctgagatc gcgccattgc actccagcct
ggacaactgg acaacaagag cgaaactctg tcccaaaaaa
N
aaaaaaaaaa CCTACCTTGA GCTGGTGGAT ATTTCTTCCC CTTAGGTATG GACCTAGGGG
AGAGTATGTG TGAGGTAACC TATTATTATA GAGGCAGTAC CCTTCCTTAG GCTGACTAGA
GATGGTCAAT TTGGATCTGG TTGAGGGTGT TCTGTTGTTT GAGGGTGTTC TGTTTTTTGT
TTTAATTTGG TTTTGGTTGT TTTTGGtttt ggttttggtt ttggaggcag gctcttgtta
tgttgcccag gctggtctca aactcctgcc ctctatcgat tctcccgcct tggcctctca
aagtgctgag attacaagca tgagccacta tgcccagccT TGGATGCCTT GTTTTAAAGA
TAAGGTTCAT AATCTATCTT GAAGGCCTTA TTCTATTTCT
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