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CCTGTAGAGCTGCGCCAAAGAAAAA[A/C]GCCAAAGTCTTCAGAAAATAAGGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 613895 | ||||||||||||||||||||
Literature Links: |
DPY19L4 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 |
DPY19L4 - dpy-19 like 4 (C. elegans) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_181787.2 | 171 | Missense Mutation | AAG,ACG | K,T 16 | NP_861452.2 | |
XM_005250894.4 | 171 | Missense Mutation | AAG,ACG | K,T 90 | XP_005250951.2 | |
XM_005250895.3 | 171 | UTR 5 | XP_005250952.1 | |||
XM_011516983.2 | 171 | Missense Mutation | AAG,ACG | K,T 16 | XP_011515285.1 | |
XM_011516984.2 | 171 | Missense Mutation | AAG,ACG | K,T 16 | XP_011515286.1 | |
XM_017013351.1 | 171 | Missense Mutation | AAG,ACG | K,T 16 | XP_016868840.1 | |
XM_017013352.1 | 171 | Missense Mutation | AAG,ACG | K,T 16 | XP_016868841.1 | |
XM_017013353.1 | 171 | Missense Mutation | AAG,ACG | K,T 16 | XP_016868842.1 | |
XM_017013354.1 | 171 | UTR 5 | XP_016868843.1 | |||
XM_017013355.1 | 171 | UTR 5 | XP_016868844.1 | |||
XM_017013356.1 | 171 | UTR 5 | XP_016868845.1 | |||
XM_017013357.1 | 171 | UTR 5 | XP_016868846.1 |