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GGTGGACTTGAAGAAGTACCTCCAG[C/T]TGTGATGGAGCGTCCGGAAAAGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608411 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
XPO6 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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XPO6 - exportin 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270940.1 | 2879 | Missense Mutation | AAC,AGC | N,S 935 | NP_001257869.1 | |
NM_015171.3 | 2879 | Missense Mutation | AAC,AGC | N,S 949 | NP_055986.1 | |
XM_005255197.3 | 2879 | Missense Mutation | AAC,AGC | N,S 875 | XP_005255254.1 | |
XM_005255198.1 | 2879 | Missense Mutation | AAC,AGC | N,S 775 | XP_005255255.1 | |
XM_005255199.2 | 2879 | Missense Mutation | AAC,AGC | N,S 604 | XP_005255256.1 | |
XM_011545772.2 | 2879 | Intron | XP_011544074.1 |