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ATAATGTCTTAAATATTTTAAGGAC[C/T]ACCTGTAGAGCTGCGCCAAAGAAAA
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 | |||
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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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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 | 144 | Missense Mutation | CCA,CTA | P,L 7 | NP_861452.2 | |
XM_005250894.4 | 144 | Missense Mutation | CCA,CTA | P,L 81 | XP_005250951.2 | |
XM_005250895.3 | 144 | UTR 5 | XP_005250952.1 | |||
XM_011516983.2 | 144 | Missense Mutation | CCA,CTA | P,L 7 | XP_011515285.1 | |
XM_011516984.2 | 144 | Missense Mutation | CCA,CTA | P,L 7 | XP_011515286.1 | |
XM_017013351.1 | 144 | Missense Mutation | CCA,CTA | P,L 7 | XP_016868840.1 | |
XM_017013352.1 | 144 | Missense Mutation | CCA,CTA | P,L 7 | XP_016868841.1 | |
XM_017013353.1 | 144 | Missense Mutation | CCA,CTA | P,L 7 | XP_016868842.1 | |
XM_017013354.1 | 144 | UTR 5 | XP_016868843.1 | |||
XM_017013355.1 | 144 | UTR 5 | XP_016868844.1 | |||
XM_017013356.1 | 144 | UTR 5 | XP_016868845.1 | |||
XM_017013357.1 | 144 | UTR 5 | XP_016868846.1 |