Search Thermo Fisher Scientific
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GCACAAATTAGAAATTCCATCATTG[C/G]AGAAAAGTATAGATGGCCTCATACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600389 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MEP1B 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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MEP1B - meprin A subunit beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308171.1 | 229 | Missense Mutation | GCA,GGA | A,G 66 | NP_001295100.1 | |
NM_005925.2 | 229 | Missense Mutation | GCA,GGA | A,G 66 | NP_005916.2 | |
XM_011526013.2 | 229 | Missense Mutation | GCA,GGA | A,G 66 | XP_011524315.1 | |
XM_011526014.2 | 229 | Missense Mutation | GCA,GGA | A,G 66 | XP_011524316.1 |