Product Details
- SNP ID
-
rs201682914
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:37251396 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTGTGCAATAATTTTTAAATCTAGG[C/T]GTCCTCCAATTCTTCAACACCAACA
- Phenotype
-
MIM: 602509
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
GOLGA4
PubMed Links
Gene Details
- Gene
- GOLGA4
- Gene Name
- golgin A4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001172713.1 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
NP_001166184.1 |
NM_002078.4 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
NP_002069.2 |
XM_005265069.3 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_005265126.1 |
XM_005265070.3 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_005265127.1 |
XM_005265071.3 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_005265128.1 |
XM_005265072.3 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_005265129.1 |
XM_005265073.1 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_005265130.1 |
XM_005265074.1 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_005265131.1 |
XM_005265075.1 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_005265132.1 |
XM_006713110.2 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_006713173.1 |
XM_011533598.2 |
434 |
Intron |
|
|
XP_011531900.1 |
XM_017006184.1 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_016861673.1 |
XM_017006185.1 |
434 |
UTR 5 |
|
|
XP_016861674.1 |
XM_017006186.1 |
434 |
UTR 5 |
|
|
XP_016861675.1 |
XM_017006187.1 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_016861676.1 |
XM_017006188.1 |
434 |
Missense Mutation |
GCG,GTG |
A25V |
XP_016861677.1 |
- Gene
- LOC152048
- Gene Name
- uncharacterized FLJ31715
There are no transcripts associated with this gene.
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