Product Details
- SNP ID
-
rs199944494
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
4
- Location
-
Chr.1:161707227 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGAGAGGTTTCATGTTGAAGAAAA[C/T]CAGTGTTGGGGTTGCAGGAGACCTA
- Phenotype
-
MIM: 606891
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FCRLA
PubMed Links
Gene Details
- Gene
- FCRLA
- Gene Name
- Fc receptor like A
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001184866.1 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
NP_001171795.1 |
NM_001184867.1 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
NP_001171796.1 |
NM_001184870.1 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
NP_001171799.1 |
NM_001184871.1 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
NP_001171800.1 |
NM_001184872.1 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
NP_001171801.1 |
NM_001184873.1 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
NP_001171802.1 |
NM_032738.3 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
NP_116127.3 |
XM_006711581.3 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
XP_006711644.1 |
XM_011510064.1 |
256 |
Intron |
|
|
XP_011508366.1 |
XM_011510065.1 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
XP_011508367.1 |
XM_011510066.1 |
256 |
Missense Mutation |
ACC,ATC |
T5I |
XP_011508368.1 |
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