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Search Thermo Fisher Scientific
GGGAGCCGCATACACGACGGGCCTG[A/C]AGCTCACGGGCACGCACACAGAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612920 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KRTAP12-1 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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KRTAP12-1 - keratin associated protein 12-1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_181686.1 | 219 | Missense Mutation | TGC,TTC | C,F 60 | NP_859014.1 |
TSPEAR - thrombospondin type laminin G domain and EAR repeats | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001272037.1 | 219 | Intron | NP_001258966.1 | |||
NM_144991.2 | 219 | Intron | NP_659428.2 |