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CCCGATGCCAACCACAAGCCAGAGA[C/T]GGCCATTGCCCTCACCCCCTTCCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 154550 | ||||||||||||||||||||
Literature Links: |
FAM219B PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
FAM219B - family with sequence similarity 219 member B | ||||||
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There are no transcripts associated with this gene. |
MPI - mannose phosphate isomerase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289155.1 | 348 | Missense Mutation | ACG,ATG | T,M 138 | NP_001276084.1 | |
NM_001289156.1 | 348 | Missense Mutation | ACG,ATG | T,M 88 | NP_001276085.1 | |
NM_001289157.1 | 348 | Missense Mutation | ACG,ATG | T,M 138 | NP_001276086.1 | |
NM_002435.2 | 348 | Missense Mutation | ACG,ATG | T,M 138 | NP_002426.1 | |
XM_011521592.1 | 348 | Missense Mutation | ACG,ATG | T,M 134 | XP_011519894.1 | |
XM_011521593.2 | 348 | Missense Mutation | ACG,ATG | T,M 118 | XP_011519895.1 | |
XM_017022207.1 | 348 | Missense Mutation | ACG,ATG | T,M 134 | XP_016877696.1 | |
XM_017022208.1 | 348 | Missense Mutation | ACG,ATG | T,M 118 | XP_016877697.1 | |
XM_017022209.1 | 348 | Missense Mutation | ACG,ATG | T,M 88 | XP_016877698.1 |