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SNP ID:
rs4954493
Gene
MCM6
Gene Name
Set Membership:
-
Chromosome Location:
Chr.2: 135852405 - 135852405 on Build GRCh38
Polymorphism:
T/C, Transition substitution
Context Sequence [VIC/FAM]:

ACTGTAAAACAGTAATTTATATTTA[T/C]CATAATGGCCTAGATGAATCCAATG

Assay ID C__29240909_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 601806

Literature Links:

 MCM6 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.35)
(0.65)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
C (0.38)
(0.62)
African American - Not Available YRI (Yoruba) - Not Available
SAS
C (0.33)
(0.67)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
C (0.13)
(0.87)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
T (0.41)
(0.59)
AMR
C (0.41)
(0.59)
MCM6 - minichromosome maintenance complex component 6
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_005915.5 Intron NP_005906.2

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