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See other MIR6845 GT Assays ›
SNP ID:
rs55807257
Gene
MIR6845 NRBP2 PUF60
Gene Name
Set Membership:
-
Chromosome Location:
Chr.8: 143837680 - 143837680 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

AGCTTCAGCGAGTGCACCTCGAAGA[A/G]CACGCGGTGGAAGAGGAGGCTGTGG

Assay ID C__90096660_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 615563 MIM: 604819

Literature Links:

 MIR6845 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.00)
(1.00)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
A (0.00)
(1.00)
African American - Not Available YRI (Yoruba) - Not Available
SAS
A (0.00)
(1.00)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
A (0.00)
(1.00)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
A (0.00)
(1.00)
AMR
A (0.00)
(1.00)
MIR6845 - microRNA 6845
There are no transcripts associated with this gene.
NRBP2 - nuclear receptor binding protein 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_178564.3 1056 Missense Mutation CTC,TTC L,F 306 NP_848659.2
XM_017013378.1 1056 Missense Mutation CTC,TTC L,F 306 XP_016868867.1
XM_017013379.1 1056 Missense Mutation CTC,TTC L,F 306 XP_016868868.1
XM_017013380.1 1056 Missense Mutation CTC,TTC L,F 306 XP_016868869.1
XM_017013381.1 1056 Missense Mutation CTC,TTC L,F 306 XP_016868870.1
XM_017013382.1 1056 Missense Mutation CTC,TTC L,F 306 XP_016868871.1
XM_017013383.1 1056 Missense Mutation CTC,TTC L,F 306 XP_016868872.1
PUF60 - poly(U) binding splicing factor 60
There are no transcripts associated with this gene.

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