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GGGGAAGGCATAACGCAGGGCCACG[A/G]AGGCGAACAGCATCTCCACGCAGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600197 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MAFK 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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MAFK - MAF bZIP transcription factor K | ||||||
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There are no transcripts associated with this gene. |
TMEM184A - transmembrane protein 184A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001097620.1 | 2259 | Missense Mutation | TCC,TTC | S,F 317 | NP_001091089.1 | |
XM_006715653.1 | 2259 | Silent Mutation | CTC,CTT | L,L 336 | XP_006715716.1 | |
XM_006715655.2 | 2259 | Missense Mutation | TCC,TTC | S,F 296 | XP_006715718.1 | |
XM_011515164.1 | 2259 | Silent Mutation | CTC,CTT | L,L 316 | XP_011513466.1 | |
XM_011515165.2 | 2259 | Silent Mutation | CTC,CTT | L,L 336 | XP_011513467.1 | |
XM_011515166.2 | 2259 | Intron | XP_011513468.1 | |||
XM_017011815.1 | 2259 | UTR 5 | XP_016867304.1 |