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AACTCTATAGGGTCACACACTGCAG[A/G]TGCAAAACCATCACAGAAAGAAGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
10 submissions
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Phenotype: |
MIM: 606625 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLAMF7 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
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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SLAMF7 - SLAM family member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282588.1 | Intron | NP_001269517.1 | ||||
NM_001282589.1 | Intron | NP_001269518.1 | ||||
NM_001282590.1 | Intron | NP_001269519.1 | ||||
NM_001282591.1 | Intron | NP_001269520.1 | ||||
NM_001282592.1 | Intron | NP_001269521.1 | ||||
NM_001282593.1 | Intron | NP_001269522.1 | ||||
NM_001282594.1 | Intron | NP_001269523.1 | ||||
NM_001282595.1 | Intron | NP_001269524.1 | ||||
NM_001282596.1 | Intron | NP_001269525.1 | ||||
NM_021181.4 | Intron | NP_067004.3 | ||||
XM_011509828.1 | Intron | XP_011508130.1 | ||||
XM_011509829.1 | Intron | XP_011508131.1 |