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AGAAGCCCAACAGGGGGGACAGGTC[C/T]AGAGAGGCAGGTATTGTTAGGTTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603044 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PLAGL1 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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PLAGL1 - PLAG1 like zinc finger 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080951.2 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001074420.1 | |
NM_001080952.2 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001074421.1 | |
NM_001080953.2 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001074422.1 | |
NM_001080954.2 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001074423.1 | |
NM_001080955.2 | 1817 | Silent Mutation | CTA,CTG | L,L 326 | NP_001074424.1 | |
NM_001080956.2 | 1817 | Silent Mutation | CTA,CTG | L,L 326 | NP_001074425.1 | |
NM_001289037.1 | 1817 | Silent Mutation | CTA,CTG | L,L 326 | NP_001275966.1 | |
NM_001289038.1 | 1817 | Silent Mutation | CTA,CTG | L,L 326 | NP_001275967.1 | |
NM_001289039.1 | 1817 | Silent Mutation | CTA,CTG | L,L 326 | NP_001275968.1 | |
NM_001289040.1 | 1817 | Silent Mutation | CTA,CTG | L,L 326 | NP_001275969.1 | |
NM_001289041.1 | 1817 | Silent Mutation | CTA,CTG | L,L 326 | NP_001275970.1 | |
NM_001289042.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001275971.1 | |
NM_001289043.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001275972.1 | |
NM_001289044.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001275973.1 | |
NM_001289045.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001275974.1 | |
NM_001289046.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001275975.1 | |
NM_001289047.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001275976.1 | |
NM_001289048.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001275977.1 | |
NM_001289049.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001275978.1 | |
NM_001317156.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001304085.1 | |
NM_001317157.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001304086.1 | |
NM_001317158.1 | 1817 | Silent Mutation | CTA,CTG | L,L 326 | NP_001304087.1 | |
NM_001317159.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001304088.1 | |
NM_001317160.1 | 1817 | Silent Mutation | CTA,CTG | L,L 326 | NP_001304089.1 | |
NM_001317161.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001304090.1 | |
NM_001317162.1 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_001304091.1 | |
NM_006718.4 | 1817 | Silent Mutation | CTA,CTG | L,L 378 | NP_006709.2 |
ZC2HC1B - zinc finger C2HC-type containing 1B | ||||||
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There are no transcripts associated with this gene. |