Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601275 | ||||||||||||||||||||||||||
Literature Links: |
GPM6A PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | CHB (Han Chinese)
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AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
GPM6A - glycoprotein M6A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001261447.1 | 1129 | Missense Mutation | GTG,TTG | V,L 207 | NP_001248376.1 | |
NM_001261448.1 | 1129 | Missense Mutation | GTG,TTG | V,L 235 | NP_001248377.1 | |
NM_005277.4 | 1129 | Missense Mutation | GTG,TTG | V,L 242 | NP_005268.1 | |
NM_201591.2 | 1129 | Missense Mutation | GTG,TTG | V,L 242 | NP_963885.1 | |
NM_201592.2 | 1129 | Missense Mutation | GTG,TTG | V,L 231 | NP_963886.1 | |
XM_006714183.1 | 1129 | Missense Mutation | GTG,TTG | V,L 179 | XP_006714246.1 | |
XM_011531877.1 | 1129 | Missense Mutation | GTG,TTG | V,L 179 | XP_011530179.1 | |
XM_017008036.1 | 1129 | Missense Mutation | GTG,TTG | V,L 179 | XP_016863525.1 |
Set Membership: |
HapMap |