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TCCTTCCAAATCTGGTAGTAAAATG[C/G]GTGCTCCAGAAAGCTGTGGCACGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C17orf51 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
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 |
C17orf51 - chromosome 17 open reading frame 51 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001113434.4 | 629 | Missense Mutation | CCC,CGC | P,R 127 | NP_001106905.1 | |
XM_005256621.3 | 629 | Intron | XP_005256678.1 | |||
XM_006721514.2 | 629 | Missense Mutation | CCC,CGC | P,R 127 | XP_006721577.1 | |
XM_011523822.2 | 629 | Missense Mutation | CCC,CGC | P,R 127 | XP_011522124.1 |