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TTTCTTTTCATTCATCACTCACCTT[A/C]TTGTCCCTAGACCTCAGCAAACTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607835 MIM: 605171 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM228B 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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FAM228B - family with sequence similarity 228 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145710.1 | 1303 | Intron | NP_001139182.1 | |||
NM_001291328.1 | 1303 | Intron | NP_001278257.1 |
SF3B6 - splicing factor 3b subunit 6 | ||||||
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There are no transcripts associated with this gene. |
TP53I3 - tumor protein p53 inducible protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206802.2 | 1303 | Intron | NP_001193731.1 | |||
NM_004881.4 | 1303 | Missense Mutation | AAG,AAT | K,N 271 | NP_004872.2 | |
NM_147184.3 | 1303 | Missense Mutation | AAG,AAT | K,N 271 | NP_671713.1 | |
XM_005264650.2 | 1303 | Missense Mutation | AAG,AAT | K,N 182 | XP_005264707.1 | |
XM_006712150.2 | 1303 | Intron | XP_006712213.1 |