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CAGCCATGACAGCCTGGGGCAAAGT[A/G]CCCAGGGGCTGGGCCAGGGTCAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604819 MIM: 607733 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR937 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
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MIR937 - microRNA 937 | ||||||
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There are no transcripts associated with this gene. |
PUF60 - poly(U) binding splicing factor 60 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136033.2 | 1178 | Silent Mutation | GGC,GGT | G,G 322 | NP_001129505.1 | |
NM_001271096.1 | 1178 | Silent Mutation | GGC,GGT | G,G 347 | NP_001258025.1 | |
NM_001271097.1 | 1178 | Silent Mutation | GGC,GGT | G,G 319 | NP_001258026.1 | |
NM_001271098.1 | 1178 | Silent Mutation | GGC,GGT | G,G 364 | NP_001258027.1 | |
NM_001271099.1 | 1178 | Silent Mutation | GGC,GGT | G,G 336 | NP_001258028.1 | |
NM_001271100.1 | 1178 | Silent Mutation | GGC,GGT | G,G 305 | NP_001258029.1 | |
NM_014281.4 | 1178 | Silent Mutation | GGC,GGT | G,G 348 | NP_055096.2 | |
NM_078480.2 | 1178 | Silent Mutation | GGC,GGT | G,G 365 | NP_510965.1 | |
XM_011516929.2 | 1178 | Silent Mutation | GGC,GGT | G,G 402 | XP_011515231.1 | |
XM_011516930.2 | 1178 | Silent Mutation | GGC,GGT | G,G 385 | XP_011515232.1 | |
XM_017013234.1 | 1178 | Silent Mutation | GGC,GGT | G,G 402 | XP_016868723.1 | |
XM_017013235.1 | 1178 | Silent Mutation | GGC,GGT | G,G 390 | XP_016868724.1 | |
XM_017013236.1 | 1178 | Silent Mutation | GGC,GGT | G,G 385 | XP_016868725.1 | |
XM_017013237.1 | 1178 | Silent Mutation | GGC,GGT | G,G 402 | XP_016868726.1 | |
XM_017013238.1 | 1178 | Silent Mutation | GGC,GGT | G,G 402 | XP_016868727.1 | |
XM_017013239.1 | 1178 | Silent Mutation | GGC,GGT | G,G 322 | XP_016868728.1 | |
XM_017013240.1 | 1178 | Silent Mutation | GGC,GGT | G,G 305 | XP_016868729.1 |
SCRIB - scribbled planar cell polarity protein | ||||||
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There are no transcripts associated with this gene. |