Product Details

SNP ID

rs60674633

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:54922725 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCATGGACCCACCAGTTGTCAAC[C/T]GGCCTAAGAAAAGCAAGACCAAGAA

Phenotype

MIM: 300132

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TRO PubMed Links

Gene Details

Gene

TRO

Gene Name

trophinin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039705.2	553	Missense Mutation	CGG,TGG	R65W	NP_001034794.1
NM_001271183.1	553	Intron			NP_001258112.1
NM_001271184.1	553	Intron			NP_001258113.1
NM_016157.3	553	Missense Mutation	CGG,TGG	R65W	NP_057241.2
NM_177556.2	553	Missense Mutation	CGG,TGG	R65W	NP_808224.1
NM_177557.2	553	Intron			NP_808225.1
XM_006724600.2	553	Missense Mutation	CGG,TGG	R65W	XP_006724663.1
XM_011530808.1	553	Missense Mutation	CGG,TGG	R65W	XP_011529110.1
XM_011530809.1	553	Missense Mutation	CGG,TGG	R65W	XP_011529111.1
XM_011530811.2	553	Missense Mutation	CGG,TGG	R65W	XP_011529113.1
XM_011530812.1	553	Missense Mutation	CGG,TGG	R65W	XP_011529114.1
XM_011530813.1	553	Missense Mutation	CGG,TGG	R65W	XP_011529115.1
XM_011530814.1	553	Missense Mutation	CGG,TGG	R21W	XP_011529116.1
XM_017029767.1	553	Missense Mutation	CGG,TGG	R65W	XP_016885256.1
XM_017029768.1	553	Missense Mutation	CGG,TGG	R21W	XP_016885257.1
XM_017029769.1	553	Missense Mutation	CGG,TGG	R65W	XP_016885258.1
XM_017029770.1	553	Missense Mutation	CGG,TGG	R65W	XP_016885259.1
XM_017029771.1	553	Missense Mutation	CGG,TGG	R65W	XP_016885260.1
XM_017029772.1	553	Missense Mutation	CGG,TGG	R21W	XP_016885261.1
XM_017029773.1	553	Missense Mutation	CGG,TGG	R21W	XP_016885262.1

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