| ID |
SNP11.06 |
| OMIM_ID |
300400
|
| Disease |
Severe combined immunodeficiency |
| Gene |
IL2RG
|
| SNP_ID |
rs52802233
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
G/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome X |
| SNP
type |
K |
| Length |
201 |
| 5'
Near Seq 30 bp |
aaagcggctccgaacacgaaacgtgtagcg |
| 3'
Near Seq 30 bp |
ttctgcccatccacactaggcaaggagaac |
| Fasta
Sequence |
>gnl|dbSNP|rs52802233|allelePos=101|totalLen=201|taxid=9606|snpclass=1|alleles='G/T'|mol=Genomic|build=128
AAGTATTGCT CCCCCAGTGG ATTGGGTGGC TCCATTCACT CCAATGCTGA GCACTTCCAC
AGAGTGGGTT AAAGCGGCTC CGAACACGAA ACGTGTAGCG
K
TTCTGCCCAT CCACACTAGG CAAGGAGAAC TTATGTCTAT AATCCACTGA TTGTTCCTTG
AGGAGAAAGA GGATGAGGGA AAGTGGGTGT CTATGAGAGA
|
