Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCAGAGCTGGGCTATCCTCCACAG[C/G]CAGGCCCACCTGCCAGCAGCTCTCA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606057 MIM: 612187 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAPGEF3 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)
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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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RAPGEF3 - Rap guanine nucleotide exchange factor 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098531.2 | 568 | Missense Mutation | CCT,GCT | P,A 16 | NP_001092001.1 | |
NM_001098532.2 | 568 | UTR 5 | NP_001092002.1 | |||
NM_006105.5 | 568 | UTR 5 | NP_006096.2 | |||
XM_005268571.3 | 568 | UTR 5 | XP_005268628.1 | |||
XM_011537752.1 | 568 | Missense Mutation | CCT,GCT | P,A 16 | XP_011536054.1 | |
XM_011537755.1 | 568 | UTR 5 | XP_011536057.1 | |||
XM_011537758.2 | 568 | UTR 5 | XP_011536060.1 | |||
XM_017018688.1 | 568 | Missense Mutation | CCT,GCT | P,A 16 | XP_016874177.1 |
SLC48A1 - solute carrier family 48 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017842.2 | 568 | Intron | NP_060312.2 | |||
XM_005269016.4 | 568 | Intron | XP_005269073.1 | |||
XM_011538558.2 | 568 | Intron | XP_011536860.1 | |||
XM_017019612.1 | 568 | Intron | XP_016875101.1 | |||
XM_017019613.1 | 568 | Intron | XP_016875102.1 | |||
XM_017019614.1 | 568 | Intron | XP_016875103.1 | |||
XM_017019615.1 | 568 | Intron | XP_016875104.1 | |||
XM_017019616.1 | 568 | Intron | XP_016875105.1 | |||
XM_017019617.1 | 568 | Intron | XP_016875106.1 |
Set Membership: |
HapMap |