|
|
| ID |
SNP11.04 |
| OMIM_ID |
300400
|
| Disease |
Severe combined immunodeficiency |
| Gene |
IL2RG
|
| SNP_ID |
rs58537905
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/A
|
| Orientation |
fwd/ |
| Chr-Number |
chromosome X |
| SNP
type |
N |
| Length |
698 |
| 5'
Near Seq 30 bp |
tgaggctctgtctcaaaaaaaaaaaaaaaa |
| 3'
Near Seq 30 bp |
gaaagaaagaaagaaaagaaaagaaaaaaa |
| Fasta
Sequence |
>gnl|dbSNP|rs58537905|allelePos=484|totalLen=698|taxid=9606|snpclass=2|alleles='-/A'|mol=Genomic|build=129
CCCACCAGTG TCATCTCTGC TACTGCCCAG TTTCTCTCTC ATCTCTTGAC TACTCAAGCC
ACACTGCTCC CTTCACTGAC TTGAATCTAA TGCCTCCCCT CTGGATCCCC TTAATGGCTT
CCTTTTGTTT ACTTGTCTAT CTGGTATCAG GAAGAGTATG GGTAGGGAAT CCCTAATGAA
AACTCACTGG TGTCAGGAAT GGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCGA
GGTGGGCAGA TCACCTGAGG TCAGGAGTTC AAGACCAGCC TGACCAACAT GGCAAAACCC
TGTCTTTACT AAAAATACAA AAATTAGCCA GGCATGGTTG TGCATGCTCC CAGCTACTTG
GGAGGCTGAA GCAGGAGAAT CACTTGAACC AGGGAGACAG AGGTCGCAGT GAGCCCAAGA
TCGCCCCACT GCACTCAAGC CTGGGCAACA GAGTGAGGCT CTGTCTCAAA AAAAAAAAAA
AAA
N
GAAAGAAAGA AAGAAAAGAA AAGAAAAAAA GAAAACTCAC TGGAGAAAAT AGGGGGGAAA
GGAGTTGGAG GAGGGAGGGT AGGGGGTGAG CAGAGAAGCT GGGAGGCAGA GAACAGGAGC
TTGATATTAG GTCCTTCTAT CTGTCTGGTT GAATCCTTTA GCCCTACTTT CTTGGCCTTA
GCTGCTACAT TCACGTCCCT AGTCACTCAC AGTC
|
|
|
