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CCACAGCATTTTAATCCATTCACCC[A/G]TTCTTTCATGGATTTATGTAACTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616888 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM221B 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
|
FAM221B - family with sequence similarity 221 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012446.3 | Intron | NP_001012448.2 | ||||
XM_006716768.3 | Intron | XP_006716831.1 |
TMEM8B - transmembrane protein 8B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042589.2 | Intron | NP_001036054.1 | ||||
NM_001042590.2 | Intron | NP_001036055.1 | ||||
NM_016446.3 | Intron | NP_057530.2 | ||||
XM_005251483.4 | Intron | XP_005251540.3 | ||||
XM_011517901.2 | Intron | XP_011516203.1 | ||||
XM_011517902.2 | Intron | XP_011516204.1 | ||||
XM_011517903.2 | Intron | XP_011516205.1 | ||||
XM_011517904.2 | Intron | XP_011516206.1 | ||||
XM_011517905.1 | Intron | XP_011516207.1 | ||||
XM_011517908.2 | Intron | XP_011516210.1 | ||||
XM_011517910.2 | Intron | XP_011516212.1 | ||||
XM_011517911.2 | Intron | XP_011516213.1 | ||||
XM_011517912.2 | Intron | XP_011516214.1 | ||||
XM_011517913.2 | Intron | XP_011516215.1 | ||||
XM_011517914.2 | Intron | XP_011516216.1 | ||||
XM_011517915.2 | Intron | XP_011516217.1 | ||||
XM_011517916.2 | Intron | XP_011516218.1 | ||||
XM_011517918.2 | Intron | XP_011516220.1 | ||||
XM_017014805.1 | Intron | XP_016870294.1 | ||||
XM_017014806.1 | Intron | XP_016870295.1 | ||||
XM_017014807.1 | Intron | XP_016870296.1 |