Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601956 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GFRA2 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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GFRA2 - GDNF family receptor alpha 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001165038.1 | 1745 | Missense Mutation | CAG,CTG | Q,L 357 | NP_001158510.1 | |
NM_001165039.1 | 1745 | Missense Mutation | CAG,CTG | Q,L 329 | NP_001158511.1 | |
NM_001495.4 | 1745 | Missense Mutation | CAG,CTG | Q,L 462 | NP_001486.4 | |
XM_006716327.3 | 1745 | Missense Mutation | CAG,CTG | Q,L 462 | XP_006716390.1 | |
XM_011544484.2 | 1745 | Missense Mutation | CAG,CTG | Q,L 462 | XP_011542786.1 |
Set Membership: |
HapMap |