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GTTACATGCTGTATTACCTTGTGCA[C/T]GATTATCTTTCTCTGAGCAGGTTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607205 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PUM2 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 - 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
|
PUM2 - pumilio RNA binding family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282752.1 | 2910 | Missense Mutation | ATG,GTG | M,V 963 | NP_001269681.1 | |
NM_001282790.1 | 2910 | Missense Mutation | ATG,GTG | M,V 940 | NP_001269719.1 | |
NM_001282791.1 | 2910 | Missense Mutation | ATG,GTG | M,V 884 | NP_001269720.1 | |
NM_015317.2 | 2910 | Missense Mutation | ATG,GTG | M,V 1019 | NP_056132.1 | |
XM_005262607.1 | 2910 | Missense Mutation | ATG,GTG | M,V 1021 | XP_005262664.1 | |
XM_005262609.1 | 2910 | Missense Mutation | ATG,GTG | M,V 942 | XP_005262666.1 | |
XM_005262610.1 | 2910 | Missense Mutation | ATG,GTG | M,V 940 | XP_005262667.1 | |
XM_006711973.1 | 2910 | Missense Mutation | ATG,GTG | M,V 1021 | XP_006712036.1 | |
XM_006711974.2 | 2910 | Missense Mutation | ATG,GTG | M,V 1021 | XP_006712037.1 | |
XM_006711975.2 | 2910 | Missense Mutation | ATG,GTG | M,V 965 | XP_006712038.1 | |
XM_011532719.1 | 2910 | Missense Mutation | ATG,GTG | M,V 1021 | XP_011531021.1 | |
XM_011532720.2 | 2910 | Missense Mutation | ATG,GTG | M,V 1021 | XP_011531022.1 | |
XM_011532721.2 | 2910 | Missense Mutation | ATG,GTG | M,V 1021 | XP_011531023.1 | |
XM_011532723.1 | 2910 | Missense Mutation | ATG,GTG | M,V 795 | XP_011531025.1 | |
XM_011532724.2 | 2910 | Intron | XP_011531026.1 | |||
XM_011532725.2 | 2910 | Intron | XP_011531027.1 | |||
XM_017003701.1 | 2910 | Missense Mutation | ATG,GTG | M,V 1019 | XP_016859190.1 | |
XM_017003702.1 | 2910 | Missense Mutation | ATG,GTG | M,V 1019 | XP_016859191.1 | |
XM_017003703.1 | 2910 | Missense Mutation | ATG,GTG | M,V 965 | XP_016859192.1 | |
XM_017003704.1 | 2910 | Missense Mutation | ATG,GTG | M,V 965 | XP_016859193.1 | |
XM_017003705.1 | 2910 | Missense Mutation | ATG,GTG | M,V 965 | XP_016859194.1 | |
XM_017003706.1 | 2910 | Missense Mutation | ATG,GTG | M,V 965 | XP_016859195.1 | |
XM_017003707.1 | 2910 | Missense Mutation | ATG,GTG | M,V 942 | XP_016859196.1 | |
XM_017003708.1 | 2910 | Missense Mutation | ATG,GTG | M,V 942 | XP_016859197.1 | |
XM_017003709.1 | 2910 | Missense Mutation | ATG,GTG | M,V 940 | XP_016859198.1 | |
XM_017003710.1 | 2910 | Missense Mutation | ATG,GTG | M,V 940 | XP_016859199.1 | |
XM_017003711.1 | 2910 | Missense Mutation | ATG,GTG | M,V 940 | XP_016859200.1 | |
XM_017003712.1 | 2910 | Missense Mutation | ATG,GTG | M,V 940 | XP_016859201.1 | |
XM_017003713.1 | 2910 | Missense Mutation | ATG,GTG | M,V 884 | XP_016859202.1 | |
XM_017003714.1 | 2910 | Missense Mutation | ATG,GTG | M,V 793 | XP_016859203.1 | |
XM_017003715.1 | 2910 | Missense Mutation | ATG,GTG | M,V 714 | XP_016859204.1 |