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ACACTCCTCTTTATTTTAAATAGTT[C/T]TGAATAATTTATACATTTTATAAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606837 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RB1CC1 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
|
RB1CC1 - RB1 inducible coiled-coil 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001083617.1 | 5665 | UTR 3 | NP_001077086.1 | |||
NM_014781.4 | 5665 | UTR 3 | NP_055596.3 | |||
XM_011517643.2 | 5665 | UTR 3 | XP_011515945.1 | |||
XM_011517644.2 | 5665 | UTR 3 | XP_011515946.1 | |||
XM_011517645.1 | 5665 | UTR 3 | XP_011515947.1 | |||
XM_011517646.2 | 5665 | UTR 3 | XP_011515948.1 | |||
XM_011517647.2 | 5665 | Intron | XP_011515949.1 | |||
XM_011517649.2 | 5665 | Intron | XP_011515951.1 | |||
XM_017014103.1 | 5665 | UTR 3 | XP_016869592.1 | |||
XM_017014104.1 | 5665 | UTR 3 | XP_016869593.1 | |||
XM_017014105.1 | 5665 | UTR 3 | XP_016869594.1 | |||
XM_017014106.1 | 5665 | UTR 3 | XP_016869595.1 | |||
XM_017014107.1 | 5665 | UTR 3 | XP_016869596.1 | |||
XM_017014108.1 | 5665 | UTR 3 | XP_016869597.1 | |||
XM_017014109.1 | 5665 | UTR 3 | XP_016869598.1 | |||
XM_017014110.1 | 5665 | UTR 3 | XP_016869599.1 | |||
XM_017014111.1 | 5665 | UTR 3 | XP_016869600.1 | |||
XM_017014112.1 | 5665 | UTR 3 | XP_016869601.1 |