Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGTTCATTAGCTGTCGCAAAAGGC[A/T]GGTGATACTCACTGATGGAAGATGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 614660 | ||||||||||||||||||||
Literature Links: |
PATL1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
PATL1 - PAT1 homolog 1, processing body mRNA decay factor | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152716.2 | 3225 | Missense Mutation | AGC,TGC | S,C 654 | NP_689929.2 | |
XM_005273833.4 | 3225 | Missense Mutation | AGC,TGC | S,C 654 | XP_005273890.1 | |
XM_005273834.1 | 3225 | Missense Mutation | AGC,TGC | S,C 624 | XP_005273891.1 | |
XM_011544811.2 | 3225 | Missense Mutation | AGC,TGC | S,C 435 | XP_011543113.1 | |
XM_017017339.1 | 3225 | Missense Mutation | AGC,TGC | S,C 435 | XP_016872828.1 |