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AATTTGTTTTCTCTTTTAGGAAAAG[C/T]GTGCAAGTATCAGTGATGCTGCCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611509 | ||||||||||||||||||||
Literature Links: |
CENPN 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 |
CENPN - centromere protein N | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100624.2 | 1117 | Missense Mutation | CGT,TGT | R,C 60 | NP_001094094.2 | |
NM_001100625.2 | 1117 | Missense Mutation | CGT,TGT | R,C 60 | NP_001094095.2 | |
NM_001270473.1 | 1117 | Missense Mutation | CGT,TGT | R,C 60 | NP_001257402.1 | |
NM_001270474.1 | 1117 | Missense Mutation | CGT,TGT | R,C 60 | NP_001257403.1 | |
NM_018455.5 | 1117 | Missense Mutation | CGT,TGT | R,C 60 | NP_060925.2 | |
XM_006721236.3 | 1117 | Missense Mutation | CGT,TGT | R,C 60 | XP_006721299.1 | |
XM_017023456.1 | 1117 | Missense Mutation | CGT,TGT | R,C 60 | XP_016878945.1 |
CMC2 - C-X9-C motif containing 2 | ||||||
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There are no transcripts associated with this gene. |