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AGCATTGGGGACTGCGGGGACGCTC[C/T]ATGTCGGGTCGCGAATCCTGACCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C6orf226 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) - Not Available | |||
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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C6orf226 - chromosome 6 open reading frame 226 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008739.1 | 31 | Missense Mutation | ATA,ATG | I,M 1 | NP_001008739.1 |
RPL7L1 - ribosomal protein L7 like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198486.3 | 31 | Intron | NP_940888.3 | |||
XM_017010780.1 | 31 | Intron | XP_016866269.1 |