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CAACGTCCAGCTGGGCTCCTAGCAC[A/G]TTCTCGTCGATCCTGGGGACAAGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602647 MIM: 603189 | ||||||||||||||||||||
Literature Links: |
NXF1 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 |
NXF1 - nuclear RNA export factor 1 | ||||||
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There are no transcripts associated with this gene. |
STX5 - syntaxin 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001244666.1 | 1078 | Missense Mutation | ACG,ATG | T,M 320 | NP_001231595.1 | |
NM_003164.4 | 1078 | Silent Mutation | AAC,AAT | N,N 307 | NP_003155.2 | |
XM_011545223.2 | 1078 | Silent Mutation | AAC,AAT | N,N 253 | XP_011543525.1 | |
XM_011545224.2 | 1078 | Silent Mutation | AAC,AAT | N,N 211 | XP_011543526.1 |