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TGGCTTCCTCAGAAAAAAGAAAAAA[A/G]TCACAGAGATTGTTTTTCAAAAATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM81B 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 |
FAM81B - family with sequence similarity 81 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152548.2 | 75 | Silent Mutation | AAA,AAG | K,K 17 | NP_689761.2 | |
XM_005271905.2 | 75 | UTR 5 | XP_005271962.2 | |||
XM_005271906.4 | 75 | Intron | XP_005271963.2 | |||
XM_005271907.3 | 75 | Silent Mutation | AAA,AAG | K,K 17 | XP_005271964.1 | |
XM_011543207.1 | 75 | Silent Mutation | AAA,AAG | K,K 17 | XP_011541509.1 | |
XM_011543208.1 | 75 | Silent Mutation | AAA,AAG | K,K 17 | XP_011541510.1 | |
XM_011543209.1 | 75 | Intron | XP_011541511.1 | |||
XM_011543210.2 | 75 | Intron | XP_011541512.1 | |||
XM_017009118.1 | 75 | Intron | XP_016864607.1 |