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CTGAAGAACAGATGGAGGGGGGCTG[C/G]TGTTGGCAAGCAGCCGAGTGTCATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611675 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM92B 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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FAM92B - family with sequence similarity 92 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198491.2 | 869 | Missense Mutation | ACC,AGC | T,S 238 | NP_940893.1 | |
XM_005255931.2 | 869 | Missense Mutation | ACC,AGC | T,S 238 | XP_005255988.1 | |
XM_011523063.1 | 869 | Missense Mutation | ACC,AGC | T,S 238 | XP_011521365.1 | |
XM_017023198.1 | 869 | Missense Mutation | ACC,AGC | T,S 238 | XP_016878687.1 |
KIAA0513 - KIAA0513 | ||||||
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There are no transcripts associated with this gene. |