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Search Thermo Fisher Scientific
GTGATATTCCACTCCTTCCTTCTCA[C/T]GGCTCTTTCGGGGCCTGGTGGTATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601114 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MPP3 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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MPP3 - membrane palmitoylated protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001932.4 | 1455 | Missense Mutation | CAT,CGT | H,R 427 | NP_001923.2 | |
XM_006721915.2 | 1455 | Missense Mutation | CAT,CGT | H,R 427 | XP_006721978.1 | |
XM_006721916.3 | 1455 | Intron | XP_006721979.1 | |||
XM_011524828.2 | 1455 | Missense Mutation | CAT,CGT | H,R 452 | XP_011523130.1 | |
XM_017024655.1 | 1455 | Intron | XP_016880144.1 | |||
XM_017024656.1 | 1455 | Missense Mutation | CAT,CGT | H,R 225 | XP_016880145.1 | |
XM_017024657.1 | 1455 | Missense Mutation | CAT,CGT | H,R 197 | XP_016880146.1 | |
XM_017024658.1 | 1455 | Intron | XP_016880147.1 | |||
XM_017024659.1 | 1455 | Intron | XP_016880148.1 | |||
XM_017024660.1 | 1455 | Intron | XP_016880149.1 |