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TTTATTTCTTTATTTTTATTTTTTG[G/T]AGAGAGTCTGGTCCCAAACTCCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM151B 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 |
FAM151B - family with sequence similarity 151 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_205548.2 | Intron | NP_991111.2 | ||||
XM_006714564.3 | Intron | XP_006714627.2 | ||||
XM_011543234.2 | Intron | XP_011541536.1 | ||||
XM_011543235.2 | Intron | XP_011541537.1 | ||||
XM_011543236.2 | Intron | XP_011541538.1 | ||||
XM_011543237.2 | Intron | XP_011541539.1 | ||||
XM_017009166.1 | Intron | XP_016864655.1 | ||||
XM_017009167.1 | Intron | XP_016864656.1 | ||||
XM_017009168.1 | Intron | XP_016864657.1 | ||||
XM_017009169.1 | Intron | XP_016864658.1 | ||||
XM_017009170.1 | Intron | XP_016864659.1 |