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ATGAGGTACAAATTATATGCTGTAG[A/G]AATTCAGCAGTGAGAGGGAGCCTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SAMD4B 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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
SAMD4B - sterile alpha motif domain containing 4B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303614.1 | 3436 | Intron | NP_001290543.1 | |||
NM_018028.3 | 3436 | Intron | NP_060498.2 | |||
XM_011527057.2 | 3436 | Intron | XP_011525359.1 | |||
XM_011527060.2 | 3436 | Intron | XP_011525362.1 | |||
XM_011527061.2 | 3436 | Intron | XP_011525363.1 | |||
XM_011527062.2 | 3436 | Intron | XP_011525364.1 | |||
XM_011527063.2 | 3436 | Intron | XP_011525365.1 | |||
XM_011527064.2 | 3436 | Intron | XP_011525366.1 | |||
XM_017026918.1 | 3436 | Intron | XP_016882407.1 | |||
XM_017026919.1 | 3436 | Intron | XP_016882408.1 | |||
XM_017026920.1 | 3436 | Intron | XP_016882409.1 | |||
XM_017026921.1 | 3436 | Intron | XP_016882410.1 | |||
XM_017026922.1 | 3436 | Intron | XP_016882411.1 | |||
XM_017026923.1 | 3436 | UTR 5 | XP_016882412.1 |