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AGTTTTTCCAAAGTTAGTAATGCTT[G/T]CTGCTGGGACTTAGCATTTCCTCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM149A 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)
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SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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FAM149A - family with sequence similarity 149 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006655.2 | Intron | NP_001006656.1 | ||||
NM_015398.2 | Intron | NP_056213.1 | ||||
XM_005262911.1 | Intron | XP_005262968.1 | ||||
XM_005262912.1 | Intron | XP_005262969.1 | ||||
XM_005262913.1 | Intron | XP_005262970.1 | ||||
XM_011531834.1 | Intron | XP_011530136.1 | ||||
XM_011531835.2 | Intron | XP_011530137.1 | ||||
XM_011531836.1 | Intron | XP_011530138.1 | ||||
XM_017007996.1 | Intron | XP_016863485.1 | ||||
XM_017007997.1 | Intron | XP_016863486.1 | ||||
XM_017007998.1 | Intron | XP_016863487.1 | ||||
XM_017007999.1 | Intron | XP_016863488.1 | ||||
XM_017008000.1 | Intron | XP_016863489.1 | ||||
XM_017008001.1 | Intron | XP_016863490.1 | ||||
XM_017008002.1 | Intron | XP_016863491.1 | ||||
XM_017008003.1 | Intron | XP_016863492.1 | ||||
XM_017008004.1 | Intron | XP_016863493.1 | ||||
XM_017008005.1 | Intron | XP_016863494.1 | ||||
XM_017008006.1 | Intron | XP_016863495.1 | ||||
XM_017008007.1 | Intron | XP_016863496.1 | ||||
XM_017008008.1 | Intron | XP_016863497.1 |
Set Membership: |
HapMap |