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SNP ID:
rs9999140
Gene
ARAP2
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.4: 36096472 - 36096472 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

GCAGCAAATACACAAATGTTCACAC[C/T]TAAAATTAGCATAAGAGAACAAAAG

Assay ID C__30546491_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 606645

Literature Links:

 ARAP2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.20)
(0.80)
Caucasian - Not Available CEPH (CEU)
T (0.01)
(0.99)
EAS
T (0.16)
(0.84)
African American - Not Available YRI (Yoruba)
C (0.45)
(0.55)
SAS
T (0.03)
(0.97)
Chinese - Not Available JPT (Japanese)
T (0.13)
(0.87)
AFR
C (0.46)
(0.54)
Japanese - Not Available CHB (Han Chinese)
T (0.23)
(0.77)
EUR
T (0.03)
(0.97)
AMR
T (0.14)
(0.86)
ARAP2 - ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_015230.3 Intron NP_056045.2
XM_017007698.1 Intron XP_016863187.1
XM_017007699.1 Intron XP_016863188.1
XM_017007700.1 Intron XP_016863189.1
XM_017007701.1 Intron XP_016863190.1
XM_017007702.1 Intron XP_016863191.1

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