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AGAAACAACTTGAAATAAGAATTTA[C/G]TTCAAGAAATGCTATTAATGCTGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611649 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM188A PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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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
|
FAM188A - family with sequence similarity 188 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318330.1 | Intron | NP_001305259.1 | ||||
NM_024948.3 | Intron | NP_079224.1 | ||||
XM_005252600.2 | Intron | XP_005252657.1 | ||||
XM_005252602.2 | Intron | XP_005252659.1 | ||||
XM_006717508.2 | Intron | XP_006717571.1 | ||||
XM_011519690.2 | Intron | XP_011517992.1 | ||||
XM_011519691.2 | Intron | XP_011517993.1 | ||||
XM_011519693.1 | Intron | XP_011517995.1 | ||||
XM_011519694.1 | Intron | XP_011517996.1 | ||||
XM_017016671.1 | Intron | XP_016872160.1 | ||||
XM_017016672.1 | Intron | XP_016872161.1 | ||||
XM_017016673.1 | Intron | XP_016872162.1 | ||||
XM_017016674.1 | Intron | XP_016872163.1 | ||||
XM_017016675.1 | Intron | XP_016872164.1 | ||||
XM_017016676.1 | Intron | XP_016872165.1 |