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CCAGGCACCATAAGCTCTAATGCGT[C/T]GGCGGCCAAATACTTGGCAGTTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610669 | ||||||||||||||||||||
Literature Links: |
FAM193A 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 |
FAM193A - family with sequence similarity 193 member A | ||||||
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There are no transcripts associated with this gene. |
TNIP2 - TNFAIP3 interacting protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001161527.1 | 1180 | Missense Mutation | AAC,GAC | N,D 258 | NP_001154999.1 | |
NM_001292016.1 | 1180 | Missense Mutation | AAC,GAC | N,D 282 | NP_001278945.1 | |
NM_024309.3 | 1180 | Missense Mutation | AAC,GAC | N,D 365 | NP_077285.3 |