Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACTATCTCTTAAGTGTTTACCGCC[A/G]CAAGATCTTTTTTGTGGCCGTGATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 610469 | ||||||||||||||||||||
Literature Links: |
AP3M2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
AP3M2 - adaptor related protein complex 3 mu 2 subunit | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134296.1 | 660 | Missense Mutation | CAC,CGC | H,R 62 | NP_001127768.1 | |
NM_006803.3 | 660 | Missense Mutation | CAC,CGC | H,R 62 | NP_006794.1 | |
XM_017012977.1 | 660 | Missense Mutation | CAC,CGC | H,R 62 | XP_016868466.1 | |
XM_017012978.1 | 660 | UTR 5 | XP_016868467.1 | |||
XM_017012979.1 | 660 | Intron | XP_016868468.1 |