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GATGACAAGTAGAAACTTACCTCTT[C/T]TTCTGTGTCGAAGATCTCACCTTCC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603703 | |||||||||||||||||||||||
Literature Links: |
RPL6 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
RPL6 - ribosomal protein L6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000970.4 | 988 | Intron | NP_000961.2 | |||
NM_001024662.2 | 988 | Intron | NP_001019833.1 | |||
NM_001320137.1 | 988 | Intron | NP_001307066.1 | |||
NM_001320138.1 | 988 | Missense Mutation | AAA,GAA | K,E 237 | NP_001307067.1 | |
NM_001320139.1 | 988 | Intron | NP_001307068.1 | |||
NM_001320140.1 | 988 | Missense Mutation | AAA,GAA | K,E 237 | NP_001307069.1 | |
NM_001320141.1 | 988 | Missense Mutation | AAA,GAA | K,E 237 | NP_001307070.1 | |
NM_001320142.1 | 988 | Intron | NP_001307071.1 | |||
XM_017019781.1 | 988 | Missense Mutation | AAA,GAA | K,E 237 | XP_016875270.1 | |
XM_017019782.1 | 988 | Intron | XP_016875271.1 |
Set Membership: |
HapMap |