Product Details
- SNP ID
-
rs55651033
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:24369731 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGGTGCTGGGGGTGGCCGTGTTCT[C/T]GAGTGTCCCAGCATCCGCATCACCT
- Phenotype
-
MIM: 602699
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NFATC4
PubMed Links
Gene Details
- Gene
- NFATC4
- Gene Name
- nuclear factor of activated T-cells 4
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001136022.2 |
654 |
Silent Mutation |
CTC,CTT |
L174L |
NP_001129494.1 |
| NM_001198965.1 |
654 |
Silent Mutation |
CTC,CTT |
L111L |
NP_001185894.1 |
| NM_001198966.2 |
654 |
Silent Mutation |
CTC,CTT |
L41L |
NP_001185895.1 |
| NM_001198967.2 |
654 |
Silent Mutation |
CTC,CTT |
L174L |
NP_001185896.1 |
| NM_001288802.1 |
654 |
Silent Mutation |
CTC,CTT |
L99L |
NP_001275731.1 |
| NM_001320043.1 |
654 |
Silent Mutation |
CTC,CTT |
L174L |
NP_001306972.1 |
| NM_004554.4 |
654 |
Silent Mutation |
CTC,CTT |
L111L |
NP_004545.2 |
| XM_011536797.2 |
654 |
Silent Mutation |
CTC,CTT |
L99L |
XP_011535099.1 |
| XM_011536798.1 |
654 |
Silent Mutation |
CTC,CTT |
L88L |
XP_011535100.1 |
| XM_011536799.2 |
654 |
Silent Mutation |
CTC,CTT |
L99L |
XP_011535101.1 |
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