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AGCGAGTCCTCCGTGCTGCTTCCAC[C/T]CACCAGCTGATAGTGGCTTGGTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 610872 | ||||||||||||||||||||
Literature Links: |
RNF19B 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 |
RNF19B - ring finger protein 19B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127361.2 | 2441 | UTR 3 | NP_001120833.1 | |||
NM_001300826.1 | 2441 | Missense Mutation | AGT,GGT | S,G 603 | NP_001287755.1 | |
NM_153341.3 | 2441 | Missense Mutation | AGT,GGT | S,G 604 | NP_699172.2 | |
XM_006710356.2 | 2441 | Missense Mutation | AGT,GGT | S,G 604 | XP_006710419.1 | |
XM_006710357.3 | 2441 | Missense Mutation | AGT,GGT | S,G 560 | XP_006710420.1 | |
XM_006710358.3 | 2441 | UTR 3 | XP_006710421.1 |