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TCTTGGGGCCATTACTCACCAGGGC[A/G]ATGACGGTGGCACCAGCTCCTGCAC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300051 MIM: 300170 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GPM6B 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) - Not Available | ||||||
EAS
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African American - Not Available | YRI (Yoruba)
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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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GPM6B - glycoprotein M6B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001001994.2 | 1166 | Silent Mutation | ATC,ATT | I,I 218 | NP_001001994.1 | |
NM_001001995.2 | 1166 | Silent Mutation | ATC,ATT | I,I 277 | NP_001001995.1 | |
NM_001001996.2 | 1166 | Silent Mutation | ATC,ATT | I,I 277 | NP_001001996.1 | |
NM_001318729.1 | 1166 | Silent Mutation | ATC,ATT | I,I 218 | NP_001305658.1 | |
NM_005278.4 | 1166 | Silent Mutation | ATC,ATT | I,I 237 | NP_005269.1 | |
XM_005274489.4 | 1166 | Silent Mutation | ATC,ATT | I,I 237 | XP_005274546.1 | |
XM_011545497.2 | 1166 | Silent Mutation | ATC,ATT | I,I 258 | XP_011543799.1 | |
XM_017029432.1 | 1166 | Silent Mutation | ATC,ATT | I,I 258 | XP_016884921.1 | |
XM_017029433.1 | 1166 | Silent Mutation | ATC,ATT | I,I 151 | XP_016884922.1 | |
XM_017029434.1 | 1166 | Silent Mutation | ATC,ATT | I,I 151 | XP_016884923.1 |
OFD1 - OFD1, centriole and centriolar satellite protein | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |