Product Details

SNP ID

rs200731683

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:102140005 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGGGAAGGTCTGTACAAGCTGCTG[C/T]CGCACTCGGAGTACAGCCGGCCCAA

Phenotype

MIM: 140571

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HSP90AA1 PubMed Links

Gene Details

Gene

HSP90AA1

Gene Name

heat shock protein 90 alpha family class A member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017963.2	154	Intron			NP_001017963.2
NM_005348.3	154	Intron			NP_005339.3
XM_011536718.2	154	Intron			XP_011535020.1

Gene

WDR20

Gene Name

WD repeat domain 20

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242414.1	154	Missense Mutation	CCG,TCG	P28S	NP_001229343.1
NM_001242415.1	154	Missense Mutation	CCG,TCG	P28S	NP_001229344.1
NM_001242416.1	154	Missense Mutation	CCG,TCG	P28S	NP_001229345.1
NM_001242417.1	154	Missense Mutation	CCG,TCG	P28S	NP_001229346.1
NM_001242418.1	154	Missense Mutation	CCG,TCG	P28S	NP_001229347.1
NM_001320130.1	154	Missense Mutation	CCG,TCG	P28S	NP_001307059.1
NM_144574.3	154	Missense Mutation	CCG,TCG	P28S	NP_653175.2
NM_181291.2	154	Missense Mutation	CCG,TCG	P28S	NP_851808.1
NM_181308.2	154	Missense Mutation	CCG,TCG	P28S	NP_851825.1
XM_006720308.1	154	Missense Mutation	CCG,TCG	P28S	XP_006720371.1
XM_006720309.1	154	Intron			XP_006720372.1
XM_006720310.1	154	Intron			XP_006720373.1
XM_006720311.1	154	Intron			XP_006720374.1
XM_006720313.2	154	UTR 5			XP_006720376.1
XM_006720318.2	154	Missense Mutation	CCG,TCG	P28S	XP_006720381.1
XM_006720320.3	154	Missense Mutation	CCG,TCG	P28S	XP_006720383.1
XM_011537335.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535637.1
XM_011537336.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535638.1
XM_011537337.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535639.1
XM_011537338.1	154	Missense Mutation	CCG,TCG	P28S	XP_011535640.1
XM_011537339.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535641.1
XM_011537340.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535642.1
XM_011537341.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535643.1
XM_011537343.1	154	UTR 5			XP_011535645.1
XM_011537344.2	154	UTR 5			XP_011535646.1
XM_011537345.1	154	UTR 5			XP_011535647.1
XM_011537346.1	154	Intron			XP_011535648.1
XM_011537347.1	154	Intron			XP_011535649.1
XM_011537352.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535654.1
XM_011537353.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535655.1
XM_011537355.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535657.1
XM_011537356.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535658.1
XM_011537358.2	154	Missense Mutation	CCG,TCG	P28S	XP_011535660.1
XM_017021766.1	154	Missense Mutation	CCG,TCG	P28S	XP_016877255.1
XM_017021767.1	154	Missense Mutation	CCG,TCG	P28S	XP_016877256.1
XM_017021768.1	154	Missense Mutation	CCG,TCG	P28S	XP_016877257.1
XM_017021770.1	154	Missense Mutation	CCG,TCG	P28S	XP_016877259.1
XM_017021771.1	154	UTR 5			XP_016877260.1
XM_017021772.1	154	Intron			XP_016877261.1
XM_017021773.1	154	Intron			XP_016877262.1
XM_017021774.1	154	Intron			XP_016877263.1
XM_017021775.1	154	Intron			XP_016877264.1
XM_017021776.1	154	Intron			XP_016877265.1
XM_017021777.1	154	Intron			XP_016877266.1
XM_017021778.1	154	Intron			XP_016877267.1
XM_017021779.1	154	Intron			XP_016877268.1
XM_017021780.1	154	Intron			XP_016877269.1
XM_017021781.1	154	UTR 5			XP_016877270.1
XM_017021782.1	154	Intron			XP_016877271.1
XM_017021783.1	154	Missense Mutation	CCG,TCG	P28S	XP_016877272.1
XM_017021784.1	154	Missense Mutation	CCG,TCG	P28S	XP_016877273.1
XM_017021785.1	154	Missense Mutation	CCG,TCG	P28S	XP_016877274.1

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