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See other C2ORF61 GT Assays ›
SNP ID:
rs815802
Gene
C2orf61 CALM2
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.2: 47164910 - 47164910 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

CGCGTACACCTTCCAGTTTCATTCC[A/G]TATTACCTCTTCCCTGGACTCAACT

Assay ID C__12035312_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 114182

Literature Links:

 C2orf61 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.10)
(0.90)
Caucasian - Not Available CEPH (CEU)
C (0.10)
(0.90)
EAS
C (0.11)
(0.89)
African American - Not Available YRI (Yoruba)
C (0.11)
(0.89)
SAS
C (0.06)
(0.94)
Chinese - Not Available JPT (Japanese)
C (0.14)
(0.86)
AFR
C (0.11)
(0.89)
Japanese - Not Available CHB (Han Chinese)
C (0.12)
(0.88)
EUR
C (0.11)
(0.89)
AMR
C (0.09)
(0.91)
C2orf61 - chromosome 2 open reading frame 61
There are no transcripts associated with this gene.
CALM2 - calmodulin 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001305624.1 Intron NP_001292553.1
NM_001305625.1 Intron NP_001292554.1
NM_001305626.1 Intron NP_001292555.1
NM_001743.5 Intron NP_001734.1

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More Information


Set Membership:

 HapMap

Panther Classification:

Molecular Function -

calmodulin-related

Gene Ontology Categories:

Function(s) Process(es)


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