Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGTAACTCTGCTTCTGTGGGATTC[C/T]GCCCAAGAGATCTCATTACAGTTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 114182 | ||||||||||||||||||||
Literature Links: |
C2orf61 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
C2orf61 - chromosome 2 open reading frame 61 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
CALM2 - calmodulin 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001305624.1 | 351 | Missense Mutation | CAG,CGG | Q,R 90 | NP_001292553.1 | |
NM_001305625.1 | 351 | Missense Mutation | CAG,CGG | Q,R 6 | NP_001292554.1 | |
NM_001305626.1 | 351 | Missense Mutation | CAG,CGG | Q,R 6 | NP_001292555.1 | |
NM_001743.5 | 351 | Missense Mutation | CAG,CGG | Q,R 42 | NP_001734.1 |