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Search Thermo Fisher Scientific
CAGGGAGCCCCCAACTGGGGGAAGC[C/T]GCCTGGCCTCCAGGTACAGGAGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605114 | ||||||||||||||||||||
Literature Links: |
MIR4325 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 |
MIR4325 - microRNA 4325 | ||||||
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There are no transcripts associated with this gene. |
SPO11 - SPO11, initiator of meiotic double stranded breaks | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012444.2 | 211 | Missense Mutation | CGC,TGC | R,C 40 | NP_036576.1 | |
NM_198265.1 | 211 | Missense Mutation | CGC,TGC | R,C 40 | NP_937998.1 | |
XM_005260379.3 | 211 | Missense Mutation | CGC,TGC | R,C 40 | XP_005260436.1 | |
XM_005260380.3 | 211 | Missense Mutation | CGC,TGC | R,C 40 | XP_005260437.1 | |
XM_005260381.3 | 211 | Missense Mutation | CGC,TGC | R,C 40 | XP_005260438.1 | |
XM_005260382.4 | 211 | Missense Mutation | CGC,TGC | R,C 40 | XP_005260439.1 | |
XM_011528756.2 | 211 | Missense Mutation | CGC,TGC | R,C 40 | XP_011527058.1 | |
XM_011528757.2 | 211 | Intron | XP_011527059.1 |