SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 364
OMIM_ID 601859
Disease AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME
Gene

FAS

SNP_ID

rs978522

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/G
Orientation fwd/T
Chr-Number 10
SNP type R
Length 601
5' Near Seq 30 bp atttcaggcactccaacagatgttggagat
3' Near Seq 30 bp ttttggacaaccatccttattcaaaccata
Fasta Sequence GGGTTACTTT AATTTGAAAA CTTTCTTAAT CCAAAACTTC TCAGGGCCCT TAGTATGCTA ATGTCAAAGG GTTGGGTAAT TATATATACT GTTCCCCAAA CTTCTTTGCC TTTGGAATCC TTTGAAGAAT CTATTGAATG AACACCTAAT GAATGCTGGT GTTCTGGGGA AAACAGTTTG GGCATCTCTA AAGGTTATTT TTATTTTACC AGCATATTCC TGAGAGTCCT CAGGCCTTCA AGGGCAAAGA AATAAAATTT TAATAATAGA ATTTCAGGCA CTCCAACAGA TGTTGGAGAT R TTTTGGACAA CCATCCTTAT TCAAACCATA CCATATAAGT TAAAGCTTCT ACTCAAAAGA TATCCTGGTT TCTGAACATT CTGAATAACA CTTAAACAAG AATCTTGACT ATGTAAAAAA ACAGGAAGAG TTAAGATTAA AAAAAAAAAA AAAAAAAAAA ACTTCTACAT CTTTTTACCA CTAAGACTTT TGTTCTTTTC CCCTTTGGTC CTAATGTTTA AAAAATGTTG TCAACCAAAT TGTTTTTACT AAATTGCAAT AAGTTGATTT TAATAACTCC CAGCTATAGT GTATATCCAT
     

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