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CCCTGGGATGGGGGAATTGAGCTTG[C/T]GCAGGTGGTCAGCCCCTGGAGGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614942 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PGS1 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
|
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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PGS1 - phosphatidylglycerophosphate synthase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024419.4 | Intron | NP_077733.3 | ||||
XM_011525487.2 | Intron | XP_011523789.1 | ||||
XM_011525488.2 | Intron | XP_011523790.1 | ||||
XM_011525489.2 | Intron | XP_011523791.1 | ||||
XM_017025357.1 | Intron | XP_016880846.1 | ||||
XM_017025358.1 | Intron | XP_016880847.1 | ||||
XM_017025359.1 | Intron | XP_016880848.1 | ||||
XM_017025360.1 | Intron | XP_016880849.1 | ||||
XM_017025361.1 | Intron | XP_016880850.1 | ||||
XM_017025362.1 | Intron | XP_016880851.1 | ||||
XM_017025363.1 | Intron | XP_016880852.1 | ||||
XM_017025364.1 | Intron | XP_016880853.1 | ||||
XM_017025365.1 | Intron | XP_016880854.1 | ||||
XM_017025366.1 | Intron | XP_016880855.1 |