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TTTCTTTAAACTGTGTAAGTCTGTG[C/G]AATGACCTAGAGGTGCTGACCCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616444 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RBM19 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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RBM19 - RNA binding motif protein 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146698.1 | 3466 | Intron | NP_001140170.1 | |||
NM_001146699.1 | 3466 | UTR 3 | NP_001140171.1 | |||
NM_016196.3 | 3466 | Intron | NP_057280.2 | |||
XM_017020280.1 | 3466 | UTR 3 | XP_016875769.1 | |||
XM_017020281.1 | 3466 | Intron | XP_016875770.1 |