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CCAGCCGCAGCAGGCACAGCACCAC[C/T]AGCAACCAGAGGCGCCCAGAGTCGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610823 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC25A42 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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SLC25A42 - solute carrier family 25 member 42 | ||||||
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There are no transcripts associated with this gene. |
TMEM161A - transmembrane protein 161A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256766.1 | 926 | Silent Mutation | CTA,CTG | L,L 216 | NP_001243695.1 | |
NM_017814.2 | 926 | Silent Mutation | CTA,CTG | L,L 319 | NP_060284.1 | |
XM_011528117.2 | 926 | Silent Mutation | CTA,CTG | L,L 117 | XP_011526419.1 | |
XM_017026916.1 | 926 | Silent Mutation | CTA,CTG | L,L 294 | XP_016882405.1 |