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Search Thermo Fisher Scientific
TTCAACTTGGTTCTCTCCTACAAGA[A/G]GCTGGAGATCTACCTGGAACCCTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610243 | ||||||||||||||||||||
Literature Links: |
ZFYVE27 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 |
ZFYVE27 - zinc finger FYVE-type containing 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002261.3 | 339 | Missense Mutation | AAG,AGG | K,R 46 | NP_001002261.1 | |
NM_001002262.3 | 339 | Missense Mutation | AAG,AGG | K,R 46 | NP_001002262.1 | |
NM_001174119.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | NP_001167590.1 | |
NM_001174120.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | NP_001167591.1 | |
NM_001174121.1 | 339 | Intron | NP_001167592.1 | |||
NM_001174122.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | NP_001167593.1 | |
NM_144588.6 | 339 | Missense Mutation | AAG,AGG | K,R 46 | NP_653189.3 | |
XM_005269502.3 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_005269559.1 | |
XM_005269503.3 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_005269560.1 | |
XM_005269504.3 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_005269561.1 | |
XM_005269505.4 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_005269562.1 | |
XM_005269506.3 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_005269563.1 | |
XM_005269508.3 | 339 | UTR 5 | XP_005269565.1 | |||
XM_005269509.3 | 339 | UTR 5 | XP_005269566.1 | |||
XM_005269510.3 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_005269567.1 | |
XM_005269511.3 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_005269568.1 | |
XM_011539252.2 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_011537554.1 | |
XM_011539253.2 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_011537555.1 | |
XM_011539254.2 | 339 | UTR 5 | XP_011537556.1 | |||
XM_011539255.2 | 339 | UTR 5 | XP_011537557.1 | |||
XM_017015644.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_016871133.1 | |
XM_017015645.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_016871134.1 | |
XM_017015646.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_016871135.1 | |
XM_017015647.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_016871136.1 | |
XM_017015648.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_016871137.1 | |
XM_017015649.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_016871138.1 | |
XM_017015650.1 | 339 | UTR 5 | XP_016871139.1 | |||
XM_017015651.1 | 339 | UTR 5 | XP_016871140.1 | |||
XM_017015652.1 | 339 | UTR 5 | XP_016871141.1 | |||
XM_017015653.1 | 339 | UTR 5 | XP_016871142.1 | |||
XM_017015654.1 | 339 | UTR 5 | XP_016871143.1 | |||
XM_017015655.1 | 339 | Missense Mutation | AAG,AGG | K,R 46 | XP_016871144.1 |