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AAAGCAGGTTGTCCTGTACAGTATC[C/T]GCAATCAGTTACGATATAGAAATAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM91A1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
FAM91A1 - family with sequence similarity 91 member A1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317917.1 | 391 | UTR 5 | NP_001304846.1 | |||
NM_001317918.1 | 391 | Missense Mutation | CGC,TGC | R,C 43 | NP_001304847.1 | |
NM_144963.3 | 391 | Missense Mutation | CGC,TGC | R,C 43 | NP_659400.2 |