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CCTTTGGGAGTGGAGGGGTGAAGAC[A/G]GGTGGAGGAGTTCCCCGGGGGAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616381 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZCCHC8 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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ZCCHC8 - zinc finger CCHC-type containing 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017612.4 | 1599 | Silent Mutation | CCC,CCT | P,P 482 | NP_060082.2 | |
XM_006719491.2 | 1599 | Silent Mutation | CCC,CCT | P,P 405 | XP_006719554.1 | |
XM_011538555.2 | 1599 | Silent Mutation | CCC,CCT | P,P 383 | XP_011536857.1 | |
XM_017019606.1 | 1599 | Silent Mutation | CCC,CCT | P,P 391 | XP_016875095.1 |