Product Details

SNP ID

rs150826975

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:19929870 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAACCGTAAACGCTGATACTTAGCC[C/T]GAATGTACAAGCTCTTCTGTACCAG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CXorf23 PubMed Links

Gene Details

Gene

CXorf23

Gene Name

chromosome X open reading frame 23

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198279.3	2188	Missense Mutation	CAG,CGG	Q645R	NP_938020.2
XM_005274473.3	2188	Missense Mutation	CAG,CGG	Q674R	XP_005274530.1
XM_005274474.3	2188	Missense Mutation	CAG,CGG	Q654R	XP_005274531.1
XM_005274475.3	2188	Missense Mutation	CAG,CGG	Q644R	XP_005274532.1
XM_011545475.2	2188	Missense Mutation	CAG,CGG	Q674R	XP_011543777.1
XM_011545476.2	2188	Missense Mutation	CAG,CGG	Q674R	XP_011543778.1
XM_011545477.2	2188	Missense Mutation	CAG,CGG	Q645R	XP_011543779.1
XM_011545478.2	2188	Intron			XP_011543780.1
XM_011545479.2	2188	Missense Mutation	CAG,CGG	Q615R	XP_011543781.1
XM_011545482.2	2188	Intron			XP_011543784.1
XM_017029390.1	2188	Missense Mutation	CAG,CGG	Q625R	XP_016884879.1
XM_017029391.1	2188	Missense Mutation	CAG,CGG	Q624R	XP_016884880.1
XM_017029392.1	2188	Intron			XP_016884881.1

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