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ACCAGTGTGGGGGCACGTAGCTGTA[C/T]GCAGGGGTTCCTTGGGCCCTATATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616316 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM168A 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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FAM168A - family with sequence similarity 168 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286050.1 | 573 | Silent Mutation | GCA,GCG | A,A 236 | NP_001272979.1 | |
NM_001286051.1 | 573 | Silent Mutation | GCA,GCG | A,A 121 | NP_001272980.1 | |
NM_015159.2 | 573 | Silent Mutation | GCA,GCG | A,A 227 | NP_055974.1 | |
XM_017017415.1 | 573 | Silent Mutation | GCA,GCG | A,A 185 | XP_016872904.1 | |
XM_017017416.1 | 573 | Silent Mutation | GCA,GCG | A,A 130 | XP_016872905.1 |