Product Details
- SNP ID
-
rs150547635
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:53873617 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTCCCCCATGATCGTGGGGTCCCCT[C/G]GGGCCCTGACACAGCCCCTGGGTCT
- Phenotype
-
MIM: 609959
MIM: 176980
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
LOC105372457
PubMed Links
Gene Details
- Gene
- LOC105372457
- Gene Name
- uncharacterized LOC105372457
There are no transcripts associated with this gene.
- Gene
- MYADM
- Gene Name
- myeloid associated differentiation marker
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001020818.2 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001018654.1 |
| NM_001020819.2 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001018655.1 |
| NM_001020820.2 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001018656.1 |
| NM_001020821.2 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001018657.1 |
| NM_001290188.1 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001277117.1 |
| NM_001290189.1 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001277118.1 |
| NM_001290190.1 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001277119.1 |
| NM_001290191.1 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001277120.1 |
| NM_001290192.1 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001277121.1 |
| NM_001290193.1 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_001277122.1 |
| NM_001290194.1 |
769 |
Intron |
|
|
NP_001277123.1 |
| NM_138373.4 |
769 |
Missense Mutation |
CGG,GGG |
R30G |
NP_612382.1 |
- Gene
- PRKCG
- Gene Name
- protein kinase C gamma
There are no transcripts associated with this gene.
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