Product Details
- SNP ID
-
rs61735068
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:54885265 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTTCCCATGCCTTTCATATCTGCCA[A/C]ATCGAGTCCTGTGATTCCCTTGGAT
- Phenotype
-
MIM: 147045
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
FCAR
PubMed Links
Gene Details
- Gene
- FCAR
- Gene Name
- Fc fragment of IgA receptor
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_002000.3 |
262 |
Missense Mutation |
AAA,ACA |
K34T |
NP_001991.1 |
NM_133269.3 |
262 |
Missense Mutation |
AAA,ACA |
K34T |
NP_579803.1 |
NM_133271.3 |
262 |
Missense Mutation |
AAA,ACA |
K34T |
NP_579805.1 |
NM_133272.3 |
262 |
Missense Mutation |
AAA,ACA |
K22T |
NP_579806.1 |
NM_133273.3 |
262 |
Missense Mutation |
AAA,ACA |
K22T |
NP_579807.1 |
NM_133274.3 |
262 |
Missense Mutation |
AAA,ACA |
K22T |
NP_579808.1 |
NM_133277.3 |
262 |
Intron |
|
|
NP_579811.1 |
NM_133278.3 |
262 |
Missense Mutation |
AAA,ACA |
K22T |
NP_579812.1 |
XM_011526625.2 |
262 |
Missense Mutation |
AAA,ACA |
K7T |
XP_011524927.1 |
XM_017026473.1 |
262 |
Missense Mutation |
AAA,ACA |
K7T |
XP_016881962.1 |
XM_017026474.1 |
262 |
Missense Mutation |
AAA,ACA |
K7T |
XP_016881963.1 |
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