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GTCTAGGGGTCCTCCTTAGAAGGGT[A/G]ACTCTTGAATATTGCGAGGATGGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610524 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ERVFRD-1 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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ERVFRD-1 - endogenous retrovirus group FRD member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_207582.2 | 2089 | Missense Mutation | TCA,TTA | S,L 536 | NP_997465.1 |
SMIM13 - small integral membrane protein 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135575.1 | 2089 | Intron | NP_001129047.1 |