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TCTTCATGGGGGCTTTGCTGGGTGG[G/T]GGCGGCAGGTCTGGCTTCTGCAAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300019 MIM: 312420 | ||||||||||||||||||||
Literature Links: |
HCFC1 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 |
HCFC1 - host cell factor C1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005334.2 | 6399 | Silent Mutation | CCA,CCC | P,P 1799 | NP_005325.2 | |
XM_006724815.2 | 6399 | Silent Mutation | CCA,CCC | P,P 1844 | XP_006724878.1 | |
XM_006724816.2 | 6399 | Silent Mutation | CCA,CCC | P,P 1843 | XP_006724879.1 | |
XM_011531147.2 | 6399 | Silent Mutation | CCA,CCC | P,P 1803 | XP_011529449.1 | |
XM_011531148.2 | 6399 | Silent Mutation | CCA,CCC | P,P 1802 | XP_011529450.1 | |
XM_017029471.1 | 6399 | Silent Mutation | CCA,CCC | P,P 1777 | XP_016884960.1 | |
XM_017029472.1 | 6399 | Silent Mutation | CCA,CCC | P,P 1540 | XP_016884961.1 |
RENBP - renin binding protein | ||||||
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There are no transcripts associated with this gene. |