Product Details

SNP ID

rs3850315

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:101656080 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGCAATGGAATTGACAAGCAGGTG[C/T]TGGTAGTCATTAGTAATAGTCATGT

Phenotype

MIM: 300363

Polymorphism

C/T, Transition 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	2092	Silent Mutation	CAA,CAG	Q503Q	NP_001269160.1
NM_014782.6	2092	Silent Mutation	CAA,CAG	Q503Q	NP_055597.1
NM_177949.3	2092	Silent Mutation	CAA,CAG	Q503Q	NP_808818.1
XM_005278109.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_005278166.1
XM_005278110.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_005278167.1
XM_005278111.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_005278168.1
XM_005278113.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_005278170.1
XM_005278114.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_005278171.1
XM_005278115.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_005278172.1
XM_005278116.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_005278173.1
XM_005278117.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_005278174.1
XM_011531071.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_011529373.1
XM_011531072.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_011529374.1
XM_017029987.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885476.1
XM_017029988.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885477.1
XM_017029989.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885478.1
XM_017029990.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885479.1
XM_017029991.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885480.1
XM_017029992.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885481.1
XM_017029993.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885482.1
XM_017029994.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885483.1
XM_017029995.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885484.1
XM_017029996.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885485.1
XM_017029997.1	2092	Silent Mutation	CAA,CAG	Q503Q	XP_016885486.1

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