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TTTGCGTTTGAAAATTAAGACCTAA[C/T]CAACAAACTTCTAATATAAAAGTAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 607201 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HNRNPR PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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HNRNPR - heterogeneous nuclear ribonucleoprotein R | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102397.2 | 5723 | Intron | NP_001095867.1 | |||
NM_001102398.2 | 5723 | UTR 3 | NP_001095868.1 | |||
NM_001102399.2 | 5723 | Intron | NP_001095869.1 | |||
NM_001297620.1 | 5723 | UTR 3 | NP_001284549.1 | |||
NM_001297621.1 | 5723 | Intron | NP_001284550.1 | |||
NM_001297622.1 | 5723 | Intron | NP_001284551.1 | |||
NM_005826.4 | 5723 | UTR 3 | NP_005817.1 | |||
XM_005245711.4 | 5723 | Intron | XP_005245768.1 | |||
XM_011540471.2 | 5723 | Intron | XP_011538773.1 | |||
XM_011540472.2 | 5723 | Intron | XP_011538774.1 | |||
XM_011540474.2 | 5723 | Intron | XP_011538776.1 | |||
XM_011540475.2 | 5723 | Intron | XP_011538777.1 | |||
XM_011540476.2 | 5723 | Intron | XP_011538778.1 | |||
XM_011540477.2 | 5723 | Intron | XP_011538779.1 | |||
XM_017000008.1 | 5723 | Intron | XP_016855497.1 | |||
XM_017000009.1 | 5723 | Intron | XP_016855498.1 | |||
XM_017000010.1 | 5723 | Intron | XP_016855499.1 |