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SNP ID:
rs7225861
Gene
CDC42EP4
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.17: 73298028 - 73298028 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

AAAAAAAAACCCAAAGTATCAAAGG[C/T]TTAAAGAAAAAGCATTCATTTCAAA

Assay ID C__30445070_20
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 605468

Literature Links:

 CDC42EP4 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.27)
(0.73)
Caucasian - Not Available CEPH (CEU)
T (0.33)
(0.67)
EAS
T (0.13)
(0.87)
African American - Not Available YRI (Yoruba)
T (0.33)
(0.67)
SAS
T (0.27)
(0.73)
Chinese - Not Available JPT (Japanese)
T (0.16)
(0.84)
AFR
T (0.34)
(0.66)
Japanese - Not Available CHB (Han Chinese)
T (0.13)
(0.87)
EUR
T (0.36)
(0.64)
AMR
T (0.22)
(0.78)
CDC42EP4 - CDC42 effector protein 4
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_012121.4 Intron NP_036253.2
XM_005257182.2 Intron XP_005257239.1

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