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GGACACTGCAGATATCAAGCCATGC[C/T]ATCTACATGGTTACAACAGCCAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600620 MIM: 616234 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FKBP1B 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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FKBP1B - FK506 binding protein 1B | ||||||
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There are no transcripts associated with this gene. |
MFSD2B - major facilitator superfamily domain containing 2B | ||||||
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There are no transcripts associated with this gene. |
WDCP - WD repeat and coiled coil containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142319.1 | 2286 | UTR 3 | NP_001135791.1 | |||
NM_025203.2 | 2286 | Missense Mutation | AGC,GGC | S,G 719 | NP_079479.1 | |
XM_017005029.1 | 2286 | Intron | XP_016860518.1 |