Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCCTTATATGGATTCCTTCATGAC[A/G]ACTCCGATGAGAATTCTGACGGAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 603231 | ||||||||||||||||||||
Literature Links: |
OR1F2P 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 |
OR1F2P - olfactory receptor family 1 subfamily F member 2 pseudogene | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
ZNF200 - zinc finger protein 200 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145446.1 | 1397 | Missense Mutation | CGT,TGT | R,C 324 | NP_001138918.1 | |
NM_001145447.1 | 1397 | Missense Mutation | CGT,TGT | R,C 324 | NP_001138919.1 | |
NM_001145448.1 | 1397 | Missense Mutation | CGT,TGT | R,C 324 | NP_001138920.1 | |
NM_003454.3 | 1397 | Missense Mutation | CGT,TGT | R,C 325 | NP_003445.2 | |
NM_198087.2 | 1397 | Missense Mutation | CGT,TGT | R,C 324 | NP_932353.1 | |
NM_198088.2 | 1397 | Missense Mutation | CGT,TGT | R,C 325 | NP_932354.1 | |
XM_005255556.1 | 1397 | Missense Mutation | CGT,TGT | R,C 325 | XP_005255613.1 | |
XM_006720940.2 | 1397 | Missense Mutation | CGT,TGT | R,C 325 | XP_006721003.1 | |
XM_006720941.2 | 1397 | Missense Mutation | CGT,TGT | R,C 325 | XP_006721004.1 | |
XM_017023647.1 | 1397 | Missense Mutation | CGT,TGT | R,C 325 | XP_016879136.1 | |
XM_017023648.1 | 1397 | Intron | XP_016879137.1 |