|
|
| ID |
SNP11.53 |
| OMIM_ID |
300400
|
| Disease |
Severe combined immunodeficiency |
| Gene |
IL2RG
|
| SNP_ID |
rs5980743
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome X |
| SNP
type |
S |
| Length |
801 |
| 5'
Near Seq 30 bp |
gtgccaggcaccgcgctaaagacatactct |
| 3'
Near Seq 30 bp |
tgtttaatcctcacaacagctcctgtgagg |
| Fasta
Sequence |
>gnl|dbSNP|rs5980743|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='C/G'|mol=Genomic|build=124
TTTTATCACC CTTCTCCCAG TTGTCCCATA TGAAATAAAG TGATTCTGTG TTCTCTGTGC
CTGTGGCTTC CTTCCATCAC CAAACCCTCT TGGGTAATCT CTCATTACTT ACTGTCTCAT
CCTTTACTCC TAAAGACCCT GCAAAACCCT CCTCTGCTAT TGTCAGCTAC CGTTCCCCTC
ATTTTTCTGG GCTTCTCCAA ATCTCACCGT TCCAGCCAGA AATACACACA GAGAAGGCTG
ATAATCAATC CCATGGAGCC AACAGAGATA ACCACGGCTT CCAATGCAAA CAGGAAAGGA
TTCTCTATAG AAAAAAGAAA AGCAAAGTGG ACCTTatatt tgttgtgccc ctactacatg
ccaggcactg gtgccaggca ccgcgctaaa gacatactct
S
tgtttaatcc tcacaacagc tcctgtgagg caggaacaat tacctccatc ttacatctta
ggaaacagaa tccaagagtt tagggatgtg gccaaggcca aagaggtagt atgtggcaca
gcctagatcc agctggttcc aaagccATCT TCACCTTGCA GGCTCTCTAG GAATGCTTCA
GGGAAATCCT ATACATTCTA TAGCCCCCTT GAGTACCCCT CAGCCTCCTT CTCAATCCAC
TCCCCTACTC TAACAACACG CTAACCCAAC CCTACACAGA AAAACCTTGA TTTCTAGAGG
TTGGGGTTAG ACAGTGTGGA GAGATGGGGC ACCAAGTTTA GGGGCTTTAG TGACAGGGAA
GTGGAGCAAA AGACAGTGGT GTTAGAAAGG CTGGGGTGTT
|
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