Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTTTCTAGCCAGCTCAGGTGAGAG[A/C]CCTGCCACAAAAAGATCAAGGTGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 179617 MIM: 611873 | ||||||||||||||||||||
Literature Links: |
RAD51 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 |
RAD51 - RAD51 recombinase | ||||||
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There are no transcripts associated with this gene. |
RMDN3 - regulator of microtubule dynamics 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304802.1 | 1489 | Missense Mutation | GGC,GTC | G,V 376 | NP_001291731.1 | |
NM_001323894.1 | 1489 | Missense Mutation | GGC,GTC | G,V 376 | NP_001310823.1 | |
NM_001323895.1 | 1489 | Missense Mutation | GGC,GTC | G,V 247 | NP_001310824.1 | |
NM_001323896.1 | 1489 | Missense Mutation | GGC,GTC | G,V 402 | NP_001310825.1 | |
NM_001323897.1 | 1489 | Missense Mutation | GGC,GTC | G,V 402 | NP_001310826.1 | |
NM_018145.2 | 1489 | Missense Mutation | GGC,GTC | G,V 376 | NP_060615.1 | |
XM_011521755.2 | 1489 | Missense Mutation | GGC,GTC | G,V 170 | XP_011520057.1 |