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ATCAGCGTGTCAATGTCGGGCATGG[A/G]CCTAAAAGTATAAAGGTAAATATGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613934 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IFT46 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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IFT46 - intraflagellar transport 46 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168618.1 | 1026 | Missense Mutation | CCC,TCC | P,S 203 | NP_001162089.1 | |
NM_020153.3 | 1026 | Missense Mutation | CCC,TCC | P,S 254 | NP_064538.3 | |
XM_011542905.2 | 1026 | Missense Mutation | CCC,TCC | P,S 254 | XP_011541207.1 | |
XM_011542906.2 | 1026 | Missense Mutation | CCC,TCC | P,S 203 | XP_011541208.1 | |
XM_017018017.1 | 1026 | Missense Mutation | CCC,TCC | P,S 254 | XP_016873506.1 | |
XM_017018018.1 | 1026 | Missense Mutation | CCC,TCC | P,S 203 | XP_016873507.1 |
TMEM25 - transmembrane protein 25 | ||||||
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There are no transcripts associated with this gene. |