Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCTAACCTCTGCAGTCTTGATGAA[A/G]CAACTGCAAATGGAGAAAAGGGCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614356 MIM: 603143 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACSS3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
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ACSS3 - acyl-CoA synthetase short-chain family member 3 | ||||||
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There are no transcripts associated with this gene. |
PPFIA2 - PTPRF interacting protein alpha 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001220473.2 | 4253 | Intron | NP_001207402.1 | |||
NM_001220474.2 | 4253 | Intron | NP_001207403.1 | |||
NM_001220475.2 | 4253 | Missense Mutation | GCT,GTT | A,V 1219 | NP_001207404.1 | |
NM_001220476.2 | 4253 | Missense Mutation | GCT,GTT | A,V 1234 | NP_001207405.1 | |
NM_001220477.2 | 4253 | Missense Mutation | GCT,GTT | A,V 1139 | NP_001207406.1 | |
NM_001220478.2 | 4253 | Missense Mutation | GCT,GTT | A,V 1135 | NP_001207407.1 | |
NM_001220479.2 | 4253 | Intron | NP_001207408.1 | |||
NM_001220480.2 | 4253 | Missense Mutation | GCT,GTT | A,V 426 | NP_001207409.1 | |
NM_001282536.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1087 | NP_001269465.1 | |
NM_003625.4 | 4253 | Missense Mutation | GCT,GTT | A,V 1240 | NP_003616.2 | |
XM_006719670.3 | 4253 | Missense Mutation | GCT,GTT | A,V 1169 | XP_006719733.1 | |
XM_011538906.2 | 4253 | Missense Mutation | GCT,GTT | A,V 1185 | XP_011537208.1 | |
XM_011538907.2 | 4253 | Missense Mutation | GCT,GTT | A,V 1216 | XP_011537209.1 | |
XM_017020079.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1243 | XP_016875568.1 | |
XM_017020080.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1240 | XP_016875569.1 | |
XM_017020081.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1237 | XP_016875570.1 | |
XM_017020082.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1234 | XP_016875571.1 | |
XM_017020083.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1233 | XP_016875572.1 | |
XM_017020084.1 | 4253 | Intron | XP_016875573.1 | |||
XM_017020085.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1230 | XP_016875574.1 | |
XM_017020086.1 | 4253 | Intron | XP_016875575.1 | |||
XM_017020087.1 | 4253 | Intron | XP_016875576.1 | |||
XM_017020088.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1225 | XP_016875577.1 | |
XM_017020089.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1225 | XP_016875578.1 | |
XM_017020090.1 | 4253 | Intron | XP_016875579.1 | |||
XM_017020091.1 | 4253 | Intron | XP_016875580.1 | |||
XM_017020092.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1222 | XP_016875581.1 | |
XM_017020093.1 | 4253 | Intron | XP_016875582.1 | |||
XM_017020094.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1218 | XP_016875583.1 | |
XM_017020095.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1216 | XP_016875584.1 | |
XM_017020096.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1215 | XP_016875585.1 | |
XM_017020097.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1213 | XP_016875586.1 | |
XM_017020098.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1212 | XP_016875587.1 | |
XM_017020099.1 | 4253 | Intron | XP_016875588.1 | |||
XM_017020100.1 | 4253 | Intron | XP_016875589.1 | |||
XM_017020101.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1209 | XP_016875590.1 | |
XM_017020102.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1209 | XP_016875591.1 | |
XM_017020103.1 | 4253 | Intron | XP_016875592.1 | |||
XM_017020104.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1206 | XP_016875593.1 | |
XM_017020105.1 | 4253 | Intron | XP_016875594.1 | |||
XM_017020106.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1203 | XP_016875595.1 | |
XM_017020107.1 | 4253 | Intron | XP_016875596.1 | |||
XM_017020108.1 | 4253 | Intron | XP_016875597.1 | |||
XM_017020109.1 | 4253 | Intron | XP_016875598.1 | |||
XM_017020110.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1197 | XP_016875599.1 | |
XM_017020111.1 | 4253 | Intron | XP_016875600.1 | |||
XM_017020112.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1166 | XP_016875601.1 | |
XM_017020113.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1160 | XP_016875602.1 | |
XM_017020114.1 | 4253 | Intron | XP_016875603.1 | |||
XM_017020115.1 | 4253 | Intron | XP_016875604.1 | |||
XM_017020116.1 | 4253 | Intron | XP_016875605.1 | |||
XM_017020117.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1144 | XP_016875606.1 | |
XM_017020118.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1143 | XP_016875607.1 | |
XM_017020119.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1145 | XP_016875608.1 | |
XM_017020120.1 | 4253 | Missense Mutation | GCT,GTT | A,V 1090 | XP_016875609.1 |