Product Details

SNP ID
rs200081596
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:101657073 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCCAGGAGGCACCGCTGCCCTGGA[A/C]GTCTCCGCTTCTCTGGGAGCTTCTG
Phenotype
MIM: 300363
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ARMCX2 PubMed Links

Gene Details

Gene
ARMCX2
Gene Name
armadillo repeat containing, X-linked 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282231.1 1099 Silent Mutation ACG,ACT T172T NP_001269160.1
NM_014782.6 1099 Silent Mutation ACG,ACT T172T NP_055597.1
NM_177949.3 1099 Silent Mutation ACG,ACT T172T NP_808818.1
XM_005278109.1 1099 Silent Mutation ACG,ACT T172T XP_005278166.1
XM_005278110.1 1099 Silent Mutation ACG,ACT T172T XP_005278167.1
XM_005278111.1 1099 Silent Mutation ACG,ACT T172T XP_005278168.1
XM_005278113.1 1099 Silent Mutation ACG,ACT T172T XP_005278170.1
XM_005278114.1 1099 Silent Mutation ACG,ACT T172T XP_005278171.1
XM_005278115.1 1099 Silent Mutation ACG,ACT T172T XP_005278172.1
XM_005278116.1 1099 Silent Mutation ACG,ACT T172T XP_005278173.1
XM_005278117.1 1099 Silent Mutation ACG,ACT T172T XP_005278174.1
XM_011531071.1 1099 Silent Mutation ACG,ACT T172T XP_011529373.1
XM_011531072.1 1099 Silent Mutation ACG,ACT T172T XP_011529374.1
XM_017029987.1 1099 Silent Mutation ACG,ACT T172T XP_016885476.1
XM_017029988.1 1099 Silent Mutation ACG,ACT T172T XP_016885477.1
XM_017029989.1 1099 Silent Mutation ACG,ACT T172T XP_016885478.1
XM_017029990.1 1099 Silent Mutation ACG,ACT T172T XP_016885479.1
XM_017029991.1 1099 Silent Mutation ACG,ACT T172T XP_016885480.1
XM_017029992.1 1099 Silent Mutation ACG,ACT T172T XP_016885481.1
XM_017029993.1 1099 Silent Mutation ACG,ACT T172T XP_016885482.1
XM_017029994.1 1099 Silent Mutation ACG,ACT T172T XP_016885483.1
XM_017029995.1 1099 Silent Mutation ACG,ACT T172T XP_016885484.1
XM_017029996.1 1099 Silent Mutation ACG,ACT T172T XP_016885485.1
XM_017029997.1 1099 Silent Mutation ACG,ACT T172T XP_016885486.1

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