Product Details
- SNP ID
-
rs138377976
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
3
- Location
-
Chr.1:204223542 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACGACAGGGGGTTTGCTGGAGGAGC[C/T]GGGGAAGCAGGGGAGGTGGGAGGGC
- Phenotype
-
MIM: 607771
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
GOLT1A
PubMed Links
Gene Details
- Gene
- GOLT1A
- Gene Name
- golgi transport 1A
There are no transcripts associated with this gene.
- Gene
- PLEKHA6
- Gene Name
- pleckstrin homology domain containing A6
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_014935.4 |
3647 |
Silent Mutation |
CCA,CCG |
P1025P |
NP_055750.2 |
| XM_005244966.4 |
3647 |
Silent Mutation |
CCA,CCG |
P1150P |
XP_005245023.2 |
| XM_005244967.4 |
3647 |
Silent Mutation |
CCA,CCG |
P1046P |
XP_005245024.2 |
| XM_005244968.4 |
3647 |
Silent Mutation |
CCA,CCG |
P1025P |
XP_005245025.2 |
| XM_006711212.3 |
3647 |
Silent Mutation |
CCA,CCG |
P1278P |
XP_006711275.1 |
| XM_006711213.3 |
3647 |
Silent Mutation |
CCA,CCG |
P1152P |
XP_006711276.2 |
| XM_006711214.3 |
3647 |
Intron |
|
|
XP_006711277.2 |
| XM_006711215.3 |
3647 |
Silent Mutation |
CCA,CCG |
P1125P |
XP_006711278.2 |
| XM_006711217.3 |
3647 |
Silent Mutation |
CCA,CCG |
P1120P |
XP_006711280.2 |
| XM_006711219.3 |
3647 |
Silent Mutation |
CCA,CCG |
P1096P |
XP_006711282.2 |
| XM_006711221.2 |
3647 |
Silent Mutation |
CCA,CCG |
P1170P |
XP_006711284.1 |
| XM_006711222.3 |
3647 |
Silent Mutation |
CCA,CCG |
P1170P |
XP_006711285.1 |
| XM_011509295.2 |
3647 |
Silent Mutation |
CCA,CCG |
P1169P |
XP_011507597.1 |
| XM_011509296.2 |
3647 |
Silent Mutation |
CCA,CCG |
P1143P |
XP_011507598.1 |
| XM_011509297.2 |
3647 |
Silent Mutation |
CCA,CCG |
P1274P |
XP_011507599.1 |
| XM_011509298.2 |
3647 |
Silent Mutation |
CCA,CCG |
P1222P |
XP_011507600.1 |
| XM_011509299.2 |
3647 |
Silent Mutation |
CCA,CCG |
P1220P |
XP_011507601.2 |
| XM_011509301.2 |
3647 |
Silent Mutation |
CCA,CCG |
P1212P |
XP_011507603.1 |
| XM_011509304.2 |
3647 |
Silent Mutation |
CCA,CCG |
P1170P |
XP_011507606.1 |
| XM_017000687.1 |
3647 |
Intron |
|
|
XP_016856176.1 |
| XM_017000688.1 |
3647 |
Intron |
|
|
XP_016856177.1 |
| XM_017000689.1 |
3647 |
Silent Mutation |
CCA,CCG |
P1105P |
XP_016856178.1 |
| XM_017000690.1 |
3647 |
Silent Mutation |
CCA,CCG |
P1192P |
XP_016856179.1 |
| XM_017000691.1 |
3647 |
Silent Mutation |
CCA,CCG |
P998P |
XP_016856180.1 |
| XM_017000692.1 |
3647 |
Silent Mutation |
CCA,CCG |
P998P |
XP_016856181.1 |
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