Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCGCACCACCATCACAACCACCACG[A/T]CGTCATCTTCGGGCCTGGGGTCCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 609959 MIM: 176980 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105372457 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
LOC105372457 - uncharacterized LOC105372457 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
MYADM - myeloid associated differentiation marker | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001020818.2 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001018654.1 | |
NM_001020819.2 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001018655.1 | |
NM_001020820.2 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001018656.1 | |
NM_001020821.2 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001018657.1 | |
NM_001290188.1 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001277117.1 | |
NM_001290189.1 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001277118.1 | |
NM_001290190.1 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001277119.1 | |
NM_001290191.1 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001277120.1 | |
NM_001290192.1 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001277121.1 | |
NM_001290193.1 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_001277122.1 | |
NM_001290194.1 | 724 | Intron | NP_001277123.1 | |||
NM_138373.4 | 724 | Missense Mutation | ACG,TCG | T,S 15 | NP_612382.1 |
PRKCG - protein kinase C gamma | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |