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TCCGCCTATCTTCCGACCCATGAAG[C/T]GCATAACCTGGAACACATGGAAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605778 MIM: 615811 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NIF3L1 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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NIF3L1 - NGG1 interacting factor 3 like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136039.2 | 531 | Missense Mutation | CGC,TGC | R,C 102 | NP_001129511.1 | |
NM_001142355.1 | 531 | Missense Mutation | CGC,TGC | R,C 75 | NP_001135827.1 | |
NM_001142356.1 | 531 | Missense Mutation | CGC,TGC | R,C 102 | NP_001135828.1 | |
NM_021824.3 | 531 | Missense Mutation | CGC,TGC | R,C 75 | NP_068596.2 | |
XM_005246742.3 | 531 | Missense Mutation | CGC,TGC | R,C 102 | XP_005246799.1 | |
XM_011511582.1 | 531 | Missense Mutation | CGC,TGC | R,C 102 | XP_011509884.1 | |
XM_011511583.1 | 531 | Missense Mutation | CGC,TGC | R,C 102 | XP_011509885.1 | |
XM_011511584.1 | 531 | Missense Mutation | CGC,TGC | R,C 102 | XP_011509886.1 | |
XM_011511585.1 | 531 | Missense Mutation | CGC,TGC | R,C 75 | XP_011509887.1 | |
XM_017004630.1 | 531 | Missense Mutation | CGC,TGC | R,C 102 | XP_016860119.1 |
PPIL3 - peptidylprolyl isomerase like 3 | ||||||
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There are no transcripts associated with this gene. |