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TTGCAACGAGAGATTGAAATAATGC[G/T]GGGTCTGCGGCATCCCAACATTGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616014 MIM: 607652 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RNF25 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
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RNF25 - ring finger protein 25 | ||||||
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There are no transcripts associated with this gene. |
STK36 - serine/threonine kinase 36 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243313.1 | 114 | Missense Mutation | CGG,CTG | R,L 56 | NP_001230242.1 | |
NM_015690.4 | 114 | Missense Mutation | CGG,CTG | R,L 56 | NP_056505.2 | |
XM_005246464.1 | 114 | Missense Mutation | CGG,CTG | R,L 56 | XP_005246521.1 | |
XM_011510959.1 | 114 | Missense Mutation | CGG,CTG | R,L 56 | XP_011509261.1 | |
XM_011510960.1 | 114 | Missense Mutation | CGG,CTG | R,L 2 | XP_011509262.1 | |
XM_011510961.1 | 114 | Intron | XP_011509263.1 | |||
XM_017003804.1 | 114 | Missense Mutation | CGG,CTG | R,L 56 | XP_016859293.1 | |
XM_017003805.1 | 114 | UTR 5 | XP_016859294.1 |