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CTGATTCCAGGAAAGTGTTTTACCA[C/T]TCTCTGCGGGAACCCTTTGTCCATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MMP27 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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MMP27 - matrix metallopeptidase 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022122.2 | 1263 | Missense Mutation | ATG,GTG | M,V 414 | NP_071405.2 | |
XM_011542948.2 | 1263 | Missense Mutation | ATG,GTG | M,V 371 | XP_011541250.1 | |
XM_011542949.2 | 1263 | Missense Mutation | ATG,GTG | M,V 360 | XP_011541251.1 | |
XM_011542950.2 | 1263 | Missense Mutation | ATG,GTG | M,V 309 | XP_011541252.1 | |
XM_017018120.1 | 1263 | Missense Mutation | ATG,GTG | M,V 413 | XP_016873609.1 |