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CATCACCGGCTAGTCCTCAGACTCC[C/T]GGGCTGTATTTCTGCTGGTGTTTTC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616091 MIM: 612166 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101929718 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)
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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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LOC101929718 - uncharacterized LOC101929718 | ||||||
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There are no transcripts associated with this gene. |
METTL17 - methyltransferase like 17 | ||||||
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There are no transcripts associated with this gene. |
SLC39A2 - solute carrier family 39 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256588.1 | 335 | Missense Mutation | CCG,CTG | P,L 48 | NP_001243517.1 | |
NM_014579.3 | 335 | Missense Mutation | CCG,CTG | P,L 48 | NP_055394.2 |
Set Membership: |
HapMap |