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GCTCTGAGTCGTATTCCAGCTCGGC[A/G]CCCACACACTTGACACCATCCAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610702 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C20orf27 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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C20orf27 - chromosome 20 open reading frame 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039140.2 | 1157 | Silent Mutation | GGC,GGT | G,G 183 | NP_001034229.1 | |
NM_001258429.1 | 1157 | Silent Mutation | GGC,GGT | G,G 158 | NP_001245358.1 | |
NM_001258430.1 | 1157 | Silent Mutation | GGC,GGT | G,G 158 | NP_001245359.1 | |
XM_011529266.2 | 1157 | Silent Mutation | GGC,GGT | G,G 142 | XP_011527568.1 |
HSPA12B - heat shock protein family A (Hsp70) member 12B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001197327.1 | 1157 | Intron | NP_001184256.1 | |||
NM_001318322.1 | 1157 | Intron | NP_001305251.1 | |||
NM_052970.4 | 1157 | Intron | NP_443202.3 | |||
XM_011529151.2 | 1157 | Intron | XP_011527453.1 | |||
XM_017027632.1 | 1157 | Intron | XP_016883121.1 | |||
XM_017027633.1 | 1157 | Intron | XP_016883122.1 | |||
XM_017027634.1 | 1157 | Intron | XP_016883123.1 | |||
XM_017027635.1 | 1157 | Intron | XP_016883124.1 |