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TCGGGGCTCACCAGCCGTGGCTGTC[A/G]GGGGAGTTGACATTGGCACCCGCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607463 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PPP1R13L 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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PPP1R13L - protein phosphatase 1 regulatory subunit 13 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142502.1 | 2262 | Silent Mutation | CCC,CCT | P,P 689 | NP_001135974.1 | |
NM_006663.3 | 2262 | Silent Mutation | CCC,CCT | P,P 689 | NP_006654.2 | |
XM_017026177.1 | 2262 | Silent Mutation | CCC,CCT | P,P 689 | XP_016881666.1 | |
XM_017026178.1 | 2262 | Silent Mutation | CCC,CCT | P,P 689 | XP_016881667.1 | |
XM_017026179.1 | 2262 | Intron | XP_016881668.1 |