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See other ARHGAP4 GT Assays ›
SNP ID:
rs387906701
Gene
ARHGAP4 NAA10 RENBP
Gene Name
Set Membership:
-
Chromosome Location:
Chr.X: 153934388 - 153934388 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

CAGAAGCTGCCCACCTGGGGCCAGG[A/G]AAGGCCATGGTAGAAGTAGTATTTC

Assay ID C_353346637_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 300023 MIM: 300013 MIM: 312420

Literature Links:

 ARHGAP4 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
ARHGAP4 - Rho GTPase activating protein 4
There are no transcripts associated with this gene.
NAA10 - N(alpha)-acetyltransferase 10, NatA catalytic subunit
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001256119.1 359 Missense Mutation CCC,TCC P,S 37 NP_001243048.1
NM_001256120.1 359 Missense Mutation CCC,TCC P,S 37 NP_001243049.1
NM_003491.3 359 Missense Mutation CCC,TCC P,S 37 NP_003482.1
RENBP - renin binding protein
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_002910.5 359 Intron NP_002901.2
XM_017029698.1 359 Intron XP_016885187.1

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