Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGATCATAAAAAACTCCACGTACC[A/G]AGAGATAGGCAGAAGACTGAAGTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 147045 | ||||||||||||||||||||
Literature Links: |
FCAR 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 |
FCAR - Fc fragment of IgA receptor | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002000.3 | 367 | Missense Mutation | CAA,CGA | Q,R 69 | NP_001991.1 | |
NM_133269.3 | 367 | Missense Mutation | CAA,CGA | Q,R 69 | NP_579803.1 | |
NM_133271.3 | 367 | Missense Mutation | CAA,CGA | Q,R 69 | NP_579805.1 | |
NM_133272.3 | 367 | Missense Mutation | CAA,CGA | Q,R 57 | NP_579806.1 | |
NM_133273.3 | 367 | Missense Mutation | CAA,CGA | Q,R 57 | NP_579807.1 | |
NM_133274.3 | 367 | Missense Mutation | CAA,CGA | Q,R 57 | NP_579808.1 | |
NM_133277.3 | 367 | Intron | NP_579811.1 | |||
NM_133278.3 | 367 | Missense Mutation | CAA,CGA | Q,R 57 | NP_579812.1 | |
XM_011526625.2 | 367 | Missense Mutation | CAA,CGA | Q,R 42 | XP_011524927.1 | |
XM_017026473.1 | 367 | Missense Mutation | CAA,CGA | Q,R 42 | XP_016881962.1 | |
XM_017026474.1 | 367 | Missense Mutation | CAA,CGA | Q,R 42 | XP_016881963.1 |