Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGAGCCTGGGCCATGGGCACCCCGG[C/G]GGTGGCTTGTCAGAAGCCACTGGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612012 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZFYVE26 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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ZFYVE26 - zinc finger FYVE-type containing 26 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015346.3 | 5293 | Missense Mutation | CCC,CGC | P,R 2529 | NP_056161.2 | |
XM_011536609.2 | 5293 | Intron | XP_011534911.1 | |||
XM_017021124.1 | 5293 | Missense Mutation | CCC,CGC | P,R 2535 | XP_016876613.1 | |
XM_017021125.1 | 5293 | Intron | XP_016876614.1 | |||
XM_017021126.1 | 5293 | Missense Mutation | CCC,CGC | P,R 2032 | XP_016876615.1 | |
XM_017021127.1 | 5293 | Missense Mutation | CCC,CGC | P,R 1760 | XP_016876616.1 | |
XM_017021128.1 | 5293 | Missense Mutation | CCC,CGC | P,R 1729 | XP_016876617.1 |