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AGGTCCTTGCACTCATGCAGGAGAT[G/T]GGAGAGCACGTTCCTATCGAAGGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616438 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PIRC66 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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PIRC66 - piwi-interacting RNA cluster 66 | ||||||
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There are no transcripts associated with this gene. |
TNFAIP8L3 - TNF alpha induced protein 8 like 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001311175.1 | 869 | Missense Mutation | AAT,CAT | N,H 136 | NP_001298104.1 | |
NM_207381.3 | 869 | Missense Mutation | AAT,CAT | N,H 224 | NP_997264.2 | |
XM_011521545.2 | 869 | Missense Mutation | AAT,CAT | N,H 150 | XP_011519847.1 | |
XM_017022168.1 | 869 | Missense Mutation | AAT,CAT | N,H 135 | XP_016877657.1 | |
XM_017022169.1 | 869 | Missense Mutation | AAT,CAT | N,H 90 | XP_016877658.1 |