Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607805 | ||||||||||||||||||||
Literature Links: |
CNNM4 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
CNNM4 - cyclin and CBS domain divalent metal cation transport mediator 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020184.3 | 761 | Missense Mutation | GCG,GGG | A,G 249 | NP_064569.3 | |
XM_005263914.3 | 761 | Missense Mutation | GCG,GGG | A,G 249 | XP_005263971.1 | |
XM_005263915.3 | 761 | Missense Mutation | GCG,GGG | A,G 249 | XP_005263972.1 | |
XM_011510955.2 | 761 | Missense Mutation | GCG,GGG | A,G 249 | XP_011509257.1 | |
XM_011510956.2 | 761 | Missense Mutation | GCG,GGG | A,G 249 | XP_011509258.1 | |
XM_017003799.1 | 761 | Intron | XP_016859288.1 |