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See other LINC00854 GT Assays ›
SNP ID:
rs138775072
Gene
LINC00854 NBR1 TMEM106A
Gene Name
Set Membership:
-
Chromosome Location:
Chr.17: 43216468 - 43216468 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

CCCCAGAATATCTTAAACATCTCCA[A/G]TGGCAACTACTACCCCATTATGGTG

Assay ID C_164453134_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 166945

Literature Links:

 LINC00854 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.00)
(1.00)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
G (0.00)
(1.00)
African American - Not Available YRI (Yoruba) - Not Available
SAS
G (0.00)
(1.00)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
G (0.00)
(1.00)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
G (0.00)
(1.00)
AMR
G (0.00)
(1.00)
LINC00854 - long intergenic non-protein coding RNA 854
There are no transcripts associated with this gene.
NBR1 - NBR1, autophagy cargo receptor
There are no transcripts associated with this gene.
TMEM106A - transmembrane protein 106A
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001291586.1 734 Missense Mutation AAT,AGT N,S 150 NP_001278515.1
NM_001291587.1 734 Missense Mutation AAT,AGT N,S 102 NP_001278516.1
NM_001291588.1 734 Intron NP_001278517.1
NM_145041.3 734 Missense Mutation AAT,AGT N,S 150 NP_659478.1
XM_006721658.2 734 Missense Mutation AAT,AGT N,S 150 XP_006721721.1
XM_006721659.3 734 Missense Mutation AAT,AGT N,S 102 XP_006721722.1
XM_011524260.1 734 Intron XP_011522562.1
XM_017024113.1 734 Missense Mutation AAT,AGT N,S 150 XP_016879602.1
XM_017024114.1 734 Missense Mutation AAT,AGT N,S 102 XP_016879603.1

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