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CCTCCAGGTCCACCGCAGCTCCGTA[T/C]ACCTCCCATGTCATGCCCTCAGCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611240 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GPRIN2 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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GPRIN2 - G protein regulated inducer of neurite outgrowth 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014696.3 | 1314 | Silent Mutation | NP_055511.2 | |||
XM_005277666.3 | 1314 | Silent Mutation | XP_005277723.1 | |||
XM_011540388.2 | 1314 | Silent Mutation | XP_011538690.1 | |||
XM_011540395.2 | 1314 | Silent Mutation | XP_011538697.1 | |||
XM_011540400.2 | 1314 | Silent Mutation | XP_011538702.1 | |||
XM_017016974.1 | 1314 | Silent Mutation | XP_016872463.1 | |||
XM_017016975.1 | 1314 | Silent Mutation | XP_016872464.1 | |||
XM_017016976.1 | 1314 | Silent Mutation | XP_016872465.1 | |||
XM_017016977.1 | 1314 | Silent Mutation | XP_016872466.1 | |||
XM_017016978.1 | 1314 | Silent Mutation | XP_016872467.1 | |||
XM_017016979.1 | 1314 | Silent Mutation | XP_016872468.1 | |||
XM_017016980.1 | 1314 | Silent Mutation | XP_016872469.1 | |||
XM_017016981.1 | 1314 | Silent Mutation | XP_016872470.1 | |||
XM_017016982.1 | 1314 | Silent Mutation | XP_016872471.1 | |||
XM_017016983.1 | 1314 | Silent Mutation | XP_016872472.1 | |||
XM_017016984.1 | 1314 | Silent Mutation | XP_016872473.1 |
LOC107984026 - arf-GAP with GTPase, ANK repeat and PH domain-containing protein 4-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017017029.1 | 1314 | Intron | XP_016872518.1 | |||
XM_017017030.1 | 1314 | Intron | XP_016872519.1 | |||
XM_017017031.1 | 1314 | Intron | XP_016872520.1 | |||
XM_017017032.1 | 1314 | Intron | XP_016872521.1 | |||
XM_017017033.1 | 1314 | Intron | XP_016872522.1 | |||
XM_017017034.1 | 1314 | Intron | XP_016872523.1 | |||
XM_017017035.1 | 1314 | Intron | XP_016872524.1 | |||
XM_017017036.1 | 1314 | Intron | XP_016872525.1 | |||
XM_017017037.1 | 1314 | Intron | XP_016872526.1 | |||
XM_017017038.1 | 1314 | Intron | XP_016872527.1 | |||
XM_017017039.1 | 1314 | Intron | XP_016872528.1 | |||
XM_017017040.1 | 1314 | Intron | XP_016872529.1 |