Product Details

SNP ID

rs17145855

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:40637102 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCATCTGAAAATCTCGAAGCCACG[C/T]AGAAGATACTTTCATCTCTGAAGAG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CXorf38 PubMed Links

Gene Details

Gene

CXorf38

Gene Name

chromosome X open reading frame 38

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_144970.2	573	Missense Mutation	ACG,GCG	T176A	NP_659407.1
XM_005272589.2	573	Missense Mutation	ACG,GCG	T176A	XP_005272646.2
XM_006724527.3	573	Missense Mutation	ACG,GCG	T176A	XP_006724590.2
XM_006724528.2	573	Missense Mutation	ACG,GCG	T131A	XP_006724591.1
XM_017029302.1	573	Missense Mutation	ACG,GCG	T187A	XP_016884791.1
XM_017029303.1	573	Missense Mutation	ACG,GCG	T131A	XP_016884792.1
XM_017029304.1	573	Missense Mutation	ACG,GCG	T57A	XP_016884793.1
XM_017029305.1	573	Missense Mutation	ACG,GCG	T57A	XP_016884794.1

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