SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 379
OMIM_ID 601859
Disease AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME
Gene

FAS

SNP_ID

rs2862833

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 10
SNP type Y
Length 1000
5' Near Seq 30 bp aagaagcat
3' Near Seq 30 bp aaagacaagttatatttagcatcagttaga
Fasta Sequence CAGACAGCAC AGACTATGAT GGCTCAGAAA AGAGAAATTA ATGAGTGAAC CCTGTGATCA CTCAGACTTT CTGCCTAAAG ACACTTTCCA GACCATAACA CAGGAGGGAA CCCTAAGCAA AGCACAACTA TCTTACCGAC Atgcttacat gttgaaatgc taatactttg ggactcatgg gttaaataga atatattact agcattaaat tGCAGAAAAG AAAGGTGGCC CACTGGCCAG CATGTAGCTA GAATGGATAA TATGCAGGAA AGAATATTTC AAAATCCTCA TTTGGCTTTC TTAATAATAA AACCTACCCC TTGAAATGTA TACTTTCTTA TCCACATTCC AGTATCTGGA ATACGAAACT GTTTGACGAA TAATCATGTG CTGTTTGGAA GAGGTCTTCT TGGCAATAGC AACCTATGGA AATAATTATT TAACTACTAA AAGGGTTAAG GTTAAAAAGG AAGTACCTTC TAAGGGATCC AAGAAGCAT Y AAAGACAAGT TATATTTAGC ATCAGTTAGA GAAAAGGAAG ACAAAACCAA AAAGCAAGCC CCTACCAAAA AAGAGAAAAC CAGAAATACC AAAAACATTA TTTAATTACG TACTTTTACC TATATTTTAT AATTCCAAAC ACAAGGGGCA AAAAAATCCT CCATAAATGG AAGTTCTTTA GGTGGTTCCA GGTATCTGCT TCAGTTTATA ACTATCTTCA CAGTTTACAT TTACAGAAAT ATAAATATTA TTTCTTAAAA TTCACATTTA ATACAAACTT TCAAAGATAT TTAAACGTAG GATAGTAGTA AGGAGAATCT TAAATCTTAG AAACTTGGGG GTATGACAAG AGCAATTCCT AAATCCAGAT GATGATTTTA CCATTGCTAT GTATAAGCTG CCATTTGTAG CAGGTTTTAC ATGGGACATT ATTGAACATT TTCGGGGGTG GGGGAAAAAT AAGAATCTAT TTTATCATCT TTGATTGCAA ACATGGGTTC
     

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