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TTCGGCAGGGCGTTGCTGTCCCCTG[A/G]TCTCGCGGGGGCTGCAGGGGTCCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608945 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FREM2 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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FREM2 - FRAS1 related extracellular matrix protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_207361.5 | 485 | Missense Mutation | GAT,GGT | D,G 59 | NP_997244.4 | |
XM_017020554.1 | 485 | Missense Mutation | GAT,GGT | D,G 59 | XP_016876043.1 |
LINC00437 - long intergenic non-protein coding RNA 437 | ||||||
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There are no transcripts associated with this gene. |