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TCCCATTATCTTCTGCAGATTTGCC[C/T]GGGCTATGAGCACCAATACAATGGT
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 |
---|---|---|
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 |
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 | 389 | Missense Mutation | CGG,TGG | R,W 148 | NP_001230242.1 | |
NM_015690.4 | 389 | Missense Mutation | CGG,TGG | R,W 148 | NP_056505.2 | |
XM_005246464.1 | 389 | Missense Mutation | CGG,TGG | R,W 148 | XP_005246521.1 | |
XM_011510959.1 | 389 | Missense Mutation | CGG,TGG | R,W 148 | XP_011509261.1 | |
XM_011510960.1 | 389 | Missense Mutation | CGG,TGG | R,W 94 | XP_011509262.1 | |
XM_011510961.1 | 389 | Intron | XP_011509263.1 | |||
XM_017003804.1 | 389 | Missense Mutation | CGG,TGG | R,W 148 | XP_016859293.1 | |
XM_017003805.1 | 389 | UTR 5 | XP_016859294.1 |