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ATGGAACCACAGGTTACTCTAAATG[C/T]GACTTTTAAAAATGAAATTCAAAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 166945 | ||||||||||||||||||||
Literature Links: |
LOC101929767 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 |
LOC101929767 - uncharacterized LOC101929767 | ||||||
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There are no transcripts associated with this gene. |
NBR1 - NBR1, autophagy cargo receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291571.1 | 477 | Missense Mutation | GCG,GTG | A,V 9 | NP_001278500.1 | |
NM_001291572.1 | 477 | Missense Mutation | GCG,GTG | A,V 9 | NP_001278501.1 | |
NM_005899.4 | 477 | Missense Mutation | GCG,GTG | A,V 9 | NP_005890.2 | |
NM_031862.3 | 477 | Missense Mutation | GCG,GTG | A,V 9 | NP_114068.1 | |
XM_006721903.1 | 477 | Missense Mutation | GCG,GTG | A,V 9 | XP_006721966.1 | |
XM_011524813.1 | 477 | Missense Mutation | GCG,GTG | A,V 9 | XP_011523115.1 | |
XM_017024642.1 | 477 | Missense Mutation | GCG,GTG | A,V 9 | XP_016880131.1 | |
XM_017024643.1 | 477 | Missense Mutation | GCG,GTG | A,V 9 | XP_016880132.1 | |
XM_017024644.1 | 477 | Missense Mutation | GCG,GTG | A,V 9 | XP_016880133.1 |