Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602709 MIM: 607608 | ||||||||||||||||||||
Literature Links: |
APBB1 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 |
APBB1 - amyloid beta precursor protein binding family B member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164.4 | 1551 | Silent Mutation | GCC,GCT | A,A 649 | NP_001155.1 | |
NM_001257319.2 | 1551 | Silent Mutation | GCC,GCT | A,A 429 | NP_001244248.1 | |
NM_001257320.2 | 1551 | Silent Mutation | GCC,GCT | A,A 390 | NP_001244249.1 | |
NM_001257321.2 | 1551 | Silent Mutation | GCC,GCT | A,A 390 | NP_001244250.1 | |
NM_001257323.2 | 1551 | Silent Mutation | GCC,GCT | A,A 427 | NP_001244252.1 | |
NM_001257325.2 | 1551 | Silent Mutation | GCC,GCT | A,A 414 | NP_001244254.1 | |
NM_001257326.2 | 1551 | Silent Mutation | GCC,GCT | A,A 390 | NP_001244255.1 | |
NM_145689.2 | 1551 | Silent Mutation | GCC,GCT | A,A 647 | NP_663722.1 | |
XM_006718209.3 | 1551 | Silent Mutation | GCC,GCT | A,A 750 | XP_006718272.2 | |
XM_006718210.3 | 1551 | Silent Mutation | GCC,GCT | A,A 745 | XP_006718273.2 | |
XM_006718211.1 | 1551 | Silent Mutation | GCC,GCT | A,A 750 | XP_006718274.1 | |
XM_006718212.3 | 1551 | Silent Mutation | GCC,GCT | A,A 654 | XP_006718275.2 | |
XM_006718213.1 | 1551 | Silent Mutation | GCC,GCT | A,A 745 | XP_006718276.1 | |
XM_006718214.3 | 1551 | Silent Mutation | GCC,GCT | A,A 652 | XP_006718277.2 | |
XM_006718215.3 | 1551 | Silent Mutation | GCC,GCT | A,A 741 | XP_006718278.3 | |
XM_011520037.2 | 1551 | Silent Mutation | GCC,GCT | A,A 486 | XP_011518339.1 | |
XM_011520038.2 | 1551 | Silent Mutation | GCC,GCT | A,A 486 | XP_011518340.1 | |
XM_011520040.2 | 1551 | Silent Mutation | GCC,GCT | A,A 390 | XP_011518342.1 | |
XM_011520042.1 | 1551 | Silent Mutation | GCC,GCT | A,A 525 | XP_011518344.1 | |
XM_017017639.1 | 1551 | Silent Mutation | GCC,GCT | A,A 654 | XP_016873128.1 | |
XM_017017640.1 | 1551 | Silent Mutation | GCC,GCT | A,A 652 | XP_016873129.1 | |
XM_017017641.1 | 1551 | Silent Mutation | GCC,GCT | A,A 647 | XP_016873130.1 | |
XM_017017642.1 | 1551 | Silent Mutation | GCC,GCT | A,A 388 | XP_016873131.1 |
SMPD1 - sphingomyelin phosphodiesterase 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000543.4 | 1551 | Intron | NP_000534.3 | |||
NM_001007593.2 | 1551 | Intron | NP_001007594.2 | |||
NM_001318087.1 | 1551 | Intron | NP_001305016.1 | |||
NM_001318088.1 | 1551 | Intron | NP_001305017.1 | |||
XM_011520303.1 | 1551 | Intron | XP_011518605.1 | |||
XM_011520304.1 | 1551 | Intron | XP_011518606.1 |