Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACTTCTGACTCCAGACTGGAGATCC[C/G]TCTCCAGGTGCAGGGTCCCGGGAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138254 | ||||||||||||||||||||
Literature Links: |
GRIN2C 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 |
GRIN2C - glutamate ionotropic receptor NMDA type subunit 2C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000835.4 | 5120 | Missense Mutation | CGG,GGG | R,G 1225 | NP_000826.2 | |
NM_001278553.1 | 5120 | Intron | NP_001265482.1 | |||
XM_006721845.3 | 5120 | Missense Mutation | CGG,GGG | R,G 1300 | XP_006721908.1 | |
XM_006721846.3 | 5120 | Missense Mutation | CGG,GGG | R,G 1299 | XP_006721909.1 | |
XM_011524686.2 | 5120 | Missense Mutation | CGG,GGG | R,G 1328 | XP_011522988.1 | |
XM_011524687.2 | 5120 | Missense Mutation | CGG,GGG | R,G 1321 | XP_011522989.1 | |
XM_011524688.2 | 5120 | Missense Mutation | CGG,GGG | R,G 1308 | XP_011522990.1 | |
XM_011524689.2 | 5120 | Missense Mutation | CGG,GGG | R,G 1254 | XP_011522991.1 | |
XM_011524692.2 | 5120 | Intron | XP_011522994.1 | |||
XM_017024544.1 | 5120 | Missense Mutation | CGG,GGG | R,G 1329 | XP_016880033.1 |
TMEM104 - transmembrane protein 104 | ||||||
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There are no transcripts associated with this gene. |