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TACTGTGAAATGATGATCACAGTCA[A/G]TTTTTTTTTTTTTGAGATGGAGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM122B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
FAM122B - family with sequence similarity 122B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166599.2 | Intron | NP_001160071.1 | ||||
NM_001166600.2 | Intron | NP_001160072.1 | ||||
NM_001170756.1 | Intron | NP_001164227.1 | ||||
NM_001170757.1 | Intron | NP_001164228.1 | ||||
NM_145284.5 | Intron | NP_660327.2 | ||||
XM_006724730.2 | Intron | XP_006724793.1 | ||||
XM_006724732.2 | Intron | XP_006724795.1 | ||||
XM_006724733.3 | Intron | XP_006724796.1 | ||||
XM_011531282.1 | Intron | XP_011529584.1 | ||||
XM_011531283.1 | Intron | XP_011529585.1 | ||||
XM_011531284.1 | Intron | XP_011529586.1 | ||||
XM_011531285.1 | Intron | XP_011529587.1 | ||||
XM_011531286.1 | Intron | XP_011529588.1 | ||||
XM_011531287.1 | Intron | XP_011529589.1 | ||||
XM_011531288.1 | Intron | XP_011529590.1 | ||||
XM_011531289.1 | Intron | XP_011529591.1 | ||||
XM_011531290.1 | Intron | XP_011529592.1 | ||||
XM_011531291.1 | Intron | XP_011529593.1 | ||||
XM_011531292.1 | Intron | XP_011529594.1 | ||||
XM_011531293.1 | Intron | XP_011529595.1 | ||||
XM_011531294.1 | Intron | XP_011529596.1 | ||||
XM_017029306.1 | Intron | XP_016884795.1 | ||||
XM_017029307.1 | Intron | XP_016884796.1 |