Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605571 MIM: 611602 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PIWIL1 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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PIWIL1 - piwi like RNA-mediated gene silencing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190971.1 | 4466 | Intron | NP_001177900.1 | |||
NM_004764.4 | 4466 | Intron | NP_004755.2 | |||
XM_011539002.2 | 4466 | Intron | XP_011537304.1 | |||
XM_011539003.2 | 4466 | Intron | XP_011537305.1 | |||
XM_011539004.2 | 4466 | Intron | XP_011537306.1 | |||
XM_011539005.1 | 4466 | Intron | XP_011537307.1 | |||
XM_011539006.2 | 4466 | Intron | XP_011537308.1 | |||
XM_017020229.1 | 4466 | Intron | XP_016875718.1 |
RIMBP2 - RIMS binding protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015347.4 | 4466 | Silent Mutation | AAC,AAT | N,N 1003 | NP_056162.4 | |
XM_011538102.1 | 4466 | Silent Mutation | AAC,AAT | N,N 1259 | XP_011536404.1 | |
XM_011538103.2 | 4466 | Silent Mutation | AAC,AAT | N,N 1380 | XP_011536405.1 | |
XM_011538104.2 | 4466 | Silent Mutation | AAC,AAT | N,N 1259 | XP_011536406.1 | |
XM_011538105.2 | 4466 | Silent Mutation | AAC,AAT | N,N 1141 | XP_011536407.1 | |
XM_011538106.2 | 4466 | Silent Mutation | AAC,AAT | N,N 1088 | XP_011536408.1 | |
XM_011538107.2 | 4466 | Intron | XP_011536409.1 | |||
XM_011538108.2 | 4466 | Intron | XP_011536410.1 | |||
XM_017019105.1 | 4466 | Silent Mutation | AAC,AAT | N,N 1259 | XP_016874594.1 | |
XM_017019106.1 | 4466 | Silent Mutation | AAC,AAT | N,N 1141 | XP_016874595.1 | |
XM_017019107.1 | 4466 | Silent Mutation | AAC,AAT | N,N 1020 | XP_016874596.1 | |
XM_017019108.1 | 4466 | Silent Mutation | AAC,AAT | N,N 1020 | XP_016874597.1 | |
XM_017019109.1 | 4466 | Silent Mutation | AAC,AAT | N,N 1020 | XP_016874598.1 | |
XM_017019110.1 | 4466 | Silent Mutation | AAC,AAT | N,N 1020 | XP_016874599.1 | |
XM_017019111.1 | 4466 | Silent Mutation | AAC,AAT | N,N 1020 | XP_016874600.1 | |
XM_017019112.1 | 4466 | Intron | XP_016874601.1 |
Set Membership: |
HapMap Validated |