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See other NEMP1 GT Assays ›
SNP ID:
rs7962771
Gene
NEMP1
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.12: 57073060 - 57073060 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

AAATAAGAAAAAAAACTGAGAAGAA[A/G]GAAGAACTAAGGCAGAATCTTATTT

Assay ID C__31186780_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 616496

Literature Links:

 NEMP1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.13)
(0.87)
Caucasian - Not Available CEPH (CEU)
A (0.08)
(0.92)
EAS
A (0.19)
(0.81)
African American - Not Available YRI (Yoruba)
A (0.08)
(0.92)
SAS
A (0.13)
(0.87)
Chinese - Not Available JPT (Japanese)
A (0.10)
(0.90)
AFR
A (0.12)
(0.88)
Japanese - Not Available CHB (Han Chinese)
A (0.15)
(0.85)
EUR
A (0.10)
(0.90)
AMR
A (0.12)
(0.88)
NEMP1 - nuclear envelope integral membrane protein 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001130963.1 Intron NP_001124435.1
NM_015257.2 Intron NP_056072.2
XM_011538056.2 Intron XP_011536358.1
XM_011538057.2 Intron XP_011536359.1
XM_011538058.2 Intron XP_011536360.1
XM_011538059.1 Intron XP_011536361.1
XM_011538060.2 Intron XP_011536362.1
XM_017019077.1 Intron XP_016874566.1
XM_017019078.1 Intron XP_016874567.1
XM_017019079.1 Intron XP_016874568.1

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More Information


Set Membership:

 HapMap

Gene Ontology Categories:

Function(s) Process(es)


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