Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGATCTCCGTGGACGGCAGGGTGT[G/T]GAAGCCCTTGATGCCCACGGGGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 602911 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CACNG2 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
|
CACNG2 - calcium voltage-gated channel auxiliary subunit gamma 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006078.3 | 647 | Missense Mutation | AAC,CAC | N,H 261 | NP_006069.1 | |
XM_017028531.1 | 647 | Missense Mutation | AAC,CAC | N,H 175 | XP_016884020.1 |