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CCTCTTATTTGGGGATGAAGTTAAA[A/G]TCCCTGTAGGAATAATCCAGGCCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
29 submissions
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Phenotype: |
MIM: 600759 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PSEN2 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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PSEN2 - presenilin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000447.2 | Intron | NP_000438.2 | ||||
NM_012486.2 | Intron | NP_036618.2 | ||||
XM_005273199.3 | Intron | XP_005273256.1 | ||||
XM_017001835.1 | Intron | XP_016857324.1 | ||||
XM_017001836.1 | Intron | XP_016857325.1 |
Set Membership: |
HapMap |