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GCTGAACAAACTCAGCTTCTCCCCA[A/G]TGGCCAAGAATGCAGAAAATGAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602954 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FNDC8 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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FNDC8 - fibronectin type III domain containing 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017559.2 | 458 | Missense Mutation | ATG,GTG | M,V 126 | NP_060029.1 |
NLE1 - notchless homolog 1 | ||||||
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There are no transcripts associated with this gene. |
RAD51D - RAD51 paralog D | ||||||
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There are no transcripts associated with this gene. |
RAD51L3-RFFL - RAD51L3-RFFL readthrough | ||||||
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There are no transcripts associated with this gene. |