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GTCATCCAGAAGTTGGGCTCTAGTC[G/T]TCTTTGGGGGTGGAATCGGGATTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609788 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RNF169 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
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RNF169 - ring finger protein 169 | ||||||
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There are no transcripts associated with this gene. |
XRRA1 - X-ray radiation resistance associated 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270380.1 | 2121 | Intron | NP_001257309.1 | |||
NM_001270381.1 | 2121 | Missense Mutation | AAG,ACG | K,T 409 | NP_001257310.1 | |
NM_182969.2 | 2121 | Missense Mutation | AAG,ACG | K,T 684 | NP_892014.1 | |
XM_005273765.2 | 2121 | Missense Mutation | AAG,ACG | K,T 692 | XP_005273822.1 | |
XM_005273770.2 | 2121 | Missense Mutation | AAG,ACG | K,T 451 | XP_005273827.1 | |
XM_011544755.1 | 2121 | Missense Mutation | AAG,ACG | K,T 677 | XP_011543057.1 | |
XM_011544756.1 | 2121 | Missense Mutation | AAG,ACG | K,T 650 | XP_011543058.1 | |
XM_011544757.1 | 2121 | Missense Mutation | AAG,ACG | K,T 635 | XP_011543059.1 | |
XM_011544758.1 | 2121 | Missense Mutation | AAG,ACG | K,T 635 | XP_011543060.1 | |
XM_011544759.1 | 2121 | Missense Mutation | AAG,ACG | K,T 627 | XP_011543061.1 | |
XM_011544760.2 | 2121 | Missense Mutation | AAG,ACG | K,T 692 | XP_011543062.1 | |
XM_011544761.1 | 2121 | Missense Mutation | AAG,ACG | K,T 611 | XP_011543063.1 | |
XM_011544762.1 | 2121 | Missense Mutation | AAG,ACG | K,T 605 | XP_011543064.1 | |
XM_011544763.1 | 2121 | Intron | XP_011543065.1 | |||
XM_011544764.1 | 2121 | Missense Mutation | AAG,ACG | K,T 580 | XP_011543066.1 | |
XM_011544765.1 | 2121 | Missense Mutation | AAG,ACG | K,T 451 | XP_011543067.1 | |
XM_011544766.2 | 2121 | Missense Mutation | AAG,ACG | K,T 529 | XP_011543068.1 | |
XM_011544767.1 | 2121 | Missense Mutation | AAG,ACG | K,T 529 | XP_011543069.1 | |
XM_011544768.1 | 2121 | Missense Mutation | AAG,ACG | K,T 529 | XP_011543070.1 | |
XM_017017221.1 | 2121 | Missense Mutation | AAG,ACG | K,T 622 | XP_016872710.1 | |
XM_017017222.1 | 2121 | Intron | XP_016872711.1 | |||
XM_017017223.1 | 2121 | Intron | XP_016872712.1 | |||
XM_017017224.1 | 2121 | Intron | XP_016872713.1 | |||
XM_017017225.1 | 2121 | Intron | XP_016872714.1 | |||
XM_017017226.1 | 2121 | Missense Mutation | AAG,ACG | K,T 451 | XP_016872715.1 | |
XM_017017227.1 | 2121 | Missense Mutation | AAG,ACG | K,T 451 | XP_016872716.1 | |
XM_017017228.1 | 2121 | Intron | XP_016872717.1 | |||
XM_017017229.1 | 2121 | Missense Mutation | AAG,ACG | K,T 394 | XP_016872718.1 | |
XM_017017230.1 | 2121 | Missense Mutation | AAG,ACG | K,T 372 | XP_016872719.1 | |
XM_017017231.1 | 2121 | Missense Mutation | AAG,ACG | K,T 364 | XP_016872720.1 | |
XM_017017232.1 | 2121 | Intron | XP_016872721.1 | |||
XM_017017233.1 | 2121 | Missense Mutation | AAG,ACG | K,T 307 | XP_016872722.1 | |
XM_017017234.1 | 2121 | Missense Mutation | AAG,ACG | K,T 307 | XP_016872723.1 |