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TCAATGTAAAACCACCGCTGGAGAA[C/G]TTCATAAGTGACCAAGGTAACACCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603667 | ||||||||||||||||||||
Literature Links: |
LOC105373738 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 |
LOC105373738 - uncharacterized LOC105373738 | ||||||
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There are no transcripts associated with this gene. |
SLC25A12 - solute carrier family 25 member 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003705.4 | 1962 | Missense Mutation | CTT,GTT | L,V 600 | NP_003696.2 | |
XM_011512070.2 | 1962 | Missense Mutation | CTT,GTT | L,V 509 | XP_011510372.1 |