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GTTTCTGGAATGCATCTGACAAAGC[A/C]TTCTGAATAGCAAGCTTCTGGGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612896 | ||||||||||||||||||||
Literature Links: |
RDM1 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 |
RDM1 - RAD52 motif containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001034836.1 | 572 | Silent Mutation | NP_001030008.1 | |||
NM_001163120.1 | 572 | Intron | NP_001156592.1 | |||
NM_001163121.1 | 572 | Intron | NP_001156593.1 | |||
NM_001163122.1 | 572 | Intron | NP_001156594.1 | |||
NM_001163124.1 | 572 | Intron | NP_001156596.1 | |||
NM_001163125.1 | 572 | Intron | NP_001156597.1 | |||
NM_001163130.1 | 572 | Silent Mutation | NP_001156602.1 | |||
NM_145654.3 | 572 | Silent Mutation | NP_663629.1 | |||
XM_011524509.2 | 572 | Missense Mutation | XP_011522811.1 | |||
XM_011524510.2 | 572 | UTR 3 | XP_011522812.1 |