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CCTTCCGAGGAGGACTGTAGCCGCC[A/C]GGCACGACCCCTCCCGCCGCCGCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612808 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LRFN2 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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LRFN2 - leucine rich repeat and fibronectin type III domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020737.2 | 3628 | Silent Mutation | CCG,CCT | P,P 739 | NP_065788.1 | |
XM_011514761.2 | 3628 | Silent Mutation | CCG,CCT | P,P 739 | XP_011513063.1 | |
XM_011514762.2 | 3628 | Silent Mutation | CCG,CCT | P,P 739 | XP_011513064.1 | |
XM_017011110.1 | 3628 | Silent Mutation | CCG,CCT | P,P 739 | XP_016866599.1 | |
XM_017011111.1 | 3628 | Intron | XP_016866600.1 |