Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AACTGATTCATTCTCCAGAATTCAA[G/T]TTGTTCTCCAACTCGGTGGTGTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM71F2 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 |
FAM71F2 - family with sequence similarity 71 member F2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012454.5 | 243 | Missense Mutation | AAG,AAT | K,N 37 | NP_001012457.3 | |
NM_001128926.3 | 243 | Missense Mutation | AAG,AAT | K,N 37 | NP_001122398.1 | |
NM_001290254.1 | 243 | UTR 5 | NP_001277183.1 | |||
NM_001290255.1 | 243 | UTR 5 | NP_001277184.1 | |||
XM_011516128.2 | 243 | Missense Mutation | AAG,AAT | K,N 37 | XP_011514430.1 | |
XM_011516129.2 | 243 | Missense Mutation | AAG,AAT | K,N 37 | XP_011514431.1 | |
XM_011516130.2 | 243 | Missense Mutation | AAG,AAT | K,N 37 | XP_011514432.1 | |
XM_011516131.2 | 243 | Missense Mutation | AAG,AAT | K,N 37 | XP_011514433.1 | |
XM_011516132.2 | 243 | Missense Mutation | AAG,AAT | K,N 37 | XP_011514434.1 | |
XM_011516134.2 | 243 | UTR 5 | XP_011514436.1 | |||
XM_011516135.2 | 243 | Intron | XP_011514437.1 | |||
XM_011516136.2 | 243 | Intron | XP_011514438.1 | |||
XM_017012147.1 | 243 | UTR 5 | XP_016867636.1 | |||
XM_017012149.1 | 243 | Missense Mutation | AAG,AAT | K,N 37 | XP_016867638.1 |