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GCTGAGTAATAATAAGGAAGAAAAC[A/G]CAAGTAAAACAGTGAAAGGAATGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM156A PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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
|
FAM156A - family with sequence similarity 156 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242489.1 | Intron | NP_001229418.1 | ||||
NM_001242490.1 | Intron | NP_001229419.1 | ||||
NM_001242491.1 | Intron | NP_001229420.1 | ||||
NM_001242492.1 | Intron | NP_001229421.1 | ||||
NM_001242493.1 | Intron | NP_001229422.1 | ||||
NM_001242494.1 | Intron | NP_001229423.1 | ||||
NM_001242495.1 | Intron | NP_001229424.1 | ||||
NM_001242496.1 | Intron | NP_001229425.1 | ||||
NM_001242497.1 | Intron | NP_001229426.1 | ||||
NM_014138.4 | Intron | NP_054857.2 | ||||
XM_006724586.3 | Intron | XP_006724649.1 | ||||
XM_006724587.3 | Intron | XP_006724650.1 | ||||
XM_011530781.1 | Intron | XP_011529083.1 | ||||
XM_011530782.1 | Intron | XP_011529084.1 | ||||
XM_011530783.1 | Intron | XP_011529085.1 | ||||
XM_011530784.2 | Intron | XP_011529086.1 | ||||
XM_017029457.1 | Intron | XP_016884946.1 | ||||
XM_017029458.1 | Intron | XP_016884947.1 |