Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGGCAACGTTTCCATTCACCCCACC[A/G]AGAGCCAACTGTAGTTAACCAGATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614121 | ||||||||||||||||||||
Literature Links: |
PAPD4 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 |
PAPD4 - PAP associated domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114393.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | NP_001107865.1 | |
NM_001114394.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | NP_001107866.1 | |
NM_001297744.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | NP_001284673.1 | |
NM_001297745.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | NP_001284674.1 | |
NM_173797.3 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | NP_776158.2 | |
XM_011543219.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541521.1 | |
XM_011543220.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541522.1 | |
XM_011543221.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541523.1 | |
XM_011543222.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541524.1 | |
XM_011543223.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541525.1 | |
XM_011543224.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541526.1 | |
XM_011543225.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541527.1 | |
XM_011543226.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541528.1 | |
XM_011543227.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541529.1 | |
XM_011543228.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541530.1 | |
XM_011543229.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541531.1 | |
XM_011543230.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541532.1 | |
XM_011543231.2 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_011541533.1 | |
XM_011543232.2 | 1137 | Intron | XP_011541534.1 | |||
XM_011543233.2 | 1137 | Intron | XP_011541535.1 | |||
XM_017009151.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864640.1 | |
XM_017009152.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864641.1 | |
XM_017009153.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864642.1 | |
XM_017009154.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864643.1 | |
XM_017009155.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864644.1 | |
XM_017009156.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864645.1 | |
XM_017009157.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864646.1 | |
XM_017009158.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864647.1 | |
XM_017009159.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864648.1 | |
XM_017009160.1 | 1137 | Missense Mutation | CAA,CGA | Q,R 98 | XP_016864649.1 | |
XM_017009161.1 | 1137 | UTR 5 | XP_016864650.1 | |||
XM_017009162.1 | 1137 | UTR 5 | XP_016864651.1 |