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TGTCTACTGTGAGAATAAGTGTGGT[A/G]CCCGCATGATGCGGCGGCTGCTGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609799 MIM: 602464 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM222B 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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FAM222B - family with sequence similarity 222 member B | ||||||
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There are no transcripts associated with this gene. |
NEK8 - NIMA related kinase 8 | ||||||
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There are no transcripts associated with this gene. |
TRAF4 - TNF receptor associated factor 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004295.3 | 648 | Missense Mutation | ACC,GCC | T,A 173 | NP_004286.2 | |
XM_011525504.2 | 648 | Missense Mutation | ACC,GCC | T,A 180 | XP_011523806.1 | |
XM_011525505.2 | 648 | Missense Mutation | ACC,GCC | T,A 164 | XP_011523807.1 | |
XM_011525506.2 | 648 | Missense Mutation | ACC,GCC | T,A 157 | XP_011523808.1 | |
XM_011525507.2 | 648 | Missense Mutation | ACC,GCC | T,A 55 | XP_011523809.1 | |
XM_011525508.2 | 648 | Missense Mutation | ACC,GCC | T,A 55 | XP_011523810.1 |