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ATGTTGGGCCTTGCAATCGTGCTGG[C/T]GGGGCGGCTGAACGAAGGGGACAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C16orf62 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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C16orf62 - chromosome 16 open reading frame 62 | ||||||
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There are no transcripts associated with this gene. |
IQCK - IQ motif containing K | ||||||
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There are no transcripts associated with this gene. |
KNOP1 - lysine rich nucleolar protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012991.2 | 1439 | Intron | NP_001013009.2 | |||
XM_005255317.4 | 1439 | Intron | XP_005255374.1 | |||
XM_006721046.3 | 1439 | Missense Mutation | ACC,GCC | T,A 394 | XP_006721109.1 | |
XM_011545855.1 | 1439 | Missense Mutation | ACC,GCC | T,A 454 | XP_011544157.1 | |
XM_017023231.1 | 1439 | Intron | XP_016878720.1 | |||
XM_017023232.1 | 1439 | Missense Mutation | ACC,GCC | T,A 371 | XP_016878721.1 |