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CTTGGCTTAAAGGGCAAGAACGTGC[A/G]GATTTATCAAATAGCCTTGAGGAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615319 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IMPACT 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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IMPACT - impact RWD domain protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018439.3 | 361 | Silent Mutation | GCA,GCG | A,A 83 | NP_060909.1 | |
XM_017025832.1 | 361 | Silent Mutation | GCA,GCG | A,A 65 | XP_016881321.1 |