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Search Thermo Fisher Scientific
TGCACGCTGGGGACGGTGGTGGTGA[C/T]GGGCGAAGTGGTGGTGGAACCTGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602296 MIM: 600592 MIM: 602955 | ||||||||||||||||||||
Literature Links: |
AP4M1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
AP4M1 - adaptor related protein complex 4 mu 1 subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004722.3 | 2233 | Intron | NP_004713.2 | |||
XM_005250689.4 | 2233 | Intron | XP_005250746.1 | |||
XM_005250690.4 | 2233 | Intron | XP_005250747.1 | |||
XM_006716175.3 | 2233 | Intron | XP_006716238.1 | |||
XM_011516685.2 | 2233 | Intron | XP_011514987.1 | |||
XM_017012790.1 | 2233 | Intron | XP_016868279.1 | |||
XM_017012791.1 | 2233 | Intron | XP_016868280.1 |
MCM7 - minichromosome maintenance complex component 7 | ||||||
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There are no transcripts associated with this gene. |
TAF6 - TATA-box binding protein associated factor 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190415.1 | 2233 | Missense Mutation | ATC,GTC | I,V 608 | NP_001177344.1 | |
NM_005641.3 | 2233 | Missense Mutation | ATC,GTC | I,V 571 | NP_005632.1 | |
NM_139315.2 | 2233 | Missense Mutation | ATC,GTC | I,V 571 | NP_647476.1 | |
XM_006716100.2 | 2233 | Missense Mutation | ATC,GTC | I,V 571 | XP_006716163.1 | |
XM_006716101.2 | 2233 | Missense Mutation | ATC,GTC | I,V 561 | XP_006716164.1 | |
XM_006716102.2 | 2233 | Missense Mutation | ATC,GTC | I,V 561 | XP_006716165.1 | |
XM_011516542.2 | 2233 | Missense Mutation | ATC,GTC | I,V 561 | XP_011514844.1 | |
XM_011516543.2 | 2233 | Missense Mutation | ATC,GTC | I,V 561 | XP_011514845.1 | |
XM_017012568.1 | 2233 | Missense Mutation | ATC,GTC | I,V 561 | XP_016868057.1 |