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AAGTGGATCCAAGTCTGCAAACAGA[C/T]TGAACCAGGCTGACATGTCTTGGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM117B 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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FAM117B - family with sequence similarity 117 member B | ||||||
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There are no transcripts associated with this gene. |
ICA1L - islet cell autoantigen 1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288622.1 | 1874 | Missense Mutation | AAT,AGT | N,S 458 | NP_001275551.1 | |
NM_001288623.1 | 1874 | Missense Mutation | AAT,AGT | N,S 458 | NP_001275552.1 | |
NM_001288624.1 | 1874 | Intron | NP_001275553.1 | |||
NM_138468.5 | 1874 | Missense Mutation | AAT,AGT | N,S 458 | NP_612477.3 |