Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616813 MIM: 606965 MIM: 109280 MIM: 614792 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
AGAP3 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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AGAP3 - ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 | ||||||
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There are no transcripts associated with this gene. |
FASTK - Fas activated serine/threonine kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258461.1 | 979 | Missense Mutation | GCC,GTC | A,V 409 | NP_001245390.1 | |
NM_006712.4 | 979 | Missense Mutation | GCC,GTC | A,V 436 | NP_006703.1 | |
NM_033015.3 | 979 | Missense Mutation | GCC,GTC | A,V 295 | NP_148936.2 | |
XM_005249932.1 | 979 | Missense Mutation | GCC,GTC | A,V 402 | XP_005249989.1 | |
XM_005249933.3 | 979 | Missense Mutation | GCC,GTC | A,V 402 | XP_005249990.1 | |
XM_011515761.2 | 979 | Missense Mutation | GCC,GTC | A,V 436 | XP_011514063.1 | |
XM_011515762.2 | 979 | Intron | XP_011514064.1 | |||
XM_011515763.1 | 979 | Missense Mutation | GCC,GTC | A,V 268 | XP_011514065.1 | |
XM_017011704.1 | 979 | Missense Mutation | GCC,GTC | A,V 375 | XP_016867193.1 | |
XM_017011705.1 | 979 | Missense Mutation | GCC,GTC | A,V 295 | XP_016867194.1 | |
XM_017011706.1 | 979 | Missense Mutation | GCC,GTC | A,V 197 | XP_016867195.1 |
SLC4A2 - solute carrier family 4 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199692.1 | 979 | Intron | NP_001186621.1 | |||
NM_001199693.1 | 979 | Intron | NP_001186622.1 | |||
NM_001199694.1 | 979 | Intron | NP_001186623.1 | |||
NM_003040.3 | 979 | Intron | NP_003031.3 | |||
XM_006716094.3 | 979 | Intron | XP_006716157.1 |
TMUB1 - transmembrane and ubiquitin like domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |