Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300628 MIM: 300547 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FRMD7 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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FRMD7 - FERM domain containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306193.1 | 982 | Missense Mutation | TCG,TTG | S,L 266 | NP_001293122.1 | |
NM_194277.2 | 982 | Missense Mutation | TCG,TTG | S,L 281 | NP_919253.1 | |
XM_017029947.1 | 982 | Missense Mutation | TCG,TTG | S,L 265 | XP_016885436.1 | |
XM_017029948.1 | 982 | Missense Mutation | TCG,TTG | S,L 196 | XP_016885437.1 | |
XM_017029949.1 | 982 | Missense Mutation | TCG,TTG | S,L 123 | XP_016885438.1 |
STK26 - serine/threonine protein kinase 26 | ||||||
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There are no transcripts associated with this gene. |