Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606908 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARFGAP2 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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ARFGAP2 - ADP ribosylation factor GTPase activating protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242832.1 | 2900 | UTR 3 | NP_001229761.1 | |||
NM_032389.4 | 2900 | UTR 3 | NP_115765.2 | |||
XM_005253166.1 | 2900 | UTR 3 | XP_005253223.1 | |||
XM_005253167.1 | 2900 | UTR 3 | XP_005253224.1 | |||
XM_005253168.2 | 2900 | UTR 3 | XP_005253225.1 | |||
XM_006718346.1 | 2900 | UTR 3 | XP_006718409.1 | |||
XM_011520405.1 | 2900 | UTR 3 | XP_011518707.1 | |||
XM_017018413.1 | 2900 | UTR 3 | XP_016873902.1 | |||
XM_017018414.1 | 2900 | UTR 3 | XP_016873903.1 | |||
XM_017018415.1 | 2900 | UTR 3 | XP_016873904.1 |
C11orf49 - chromosome 11 open reading frame 49 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003676.2 | 2900 | Intron | NP_001003676.1 | |||
NM_001003677.2 | 2900 | Intron | NP_001003677.1 | |||
NM_001003678.2 | 2900 | Intron | NP_001003678.1 | |||
NM_001278222.1 | 2900 | Intron | NP_001265151.1 | |||
NM_024113.4 | 2900 | Intron | NP_077018.1 | |||
XM_006718315.1 | 2900 | Intron | XP_006718378.1 | |||
XM_011520364.2 | 2900 | Intron | XP_011518666.1 | |||
XM_011520365.2 | 2900 | Intron | XP_011518667.1 | |||
XM_017018276.1 | 2900 | Intron | XP_016873765.1 | |||
XM_017018277.1 | 2900 | Intron | XP_016873766.1 | |||
XM_017018278.1 | 2900 | Intron | XP_016873767.1 | |||
XM_017018279.1 | 2900 | Intron | XP_016873768.1 | |||
XM_017018280.1 | 2900 | Intron | XP_016873769.1 | |||
XM_017018281.1 | 2900 | Intron | XP_016873770.1 | |||
XM_017018282.1 | 2900 | Intron | XP_016873771.1 |
Set Membership: |
HapMap Validated |