Product Details

SNP ID

rs183963526

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:99547322 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTGAAATATATCATTGTTTTTCCC[C/G]TGCATTTTCAGGCTTAATTCATTAA

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM200A PubMed Links

Gene Details

Gene

FAM200A

Gene Name

family with sequence similarity 200 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145111.3	1270	Missense Mutation	CAC,CAG	H362Q	NP_659802.1
XM_011515911.2	1270	Missense Mutation	CAC,CAG	H362Q	XP_011514213.1
XM_011515913.2	1270	Missense Mutation	CAC,CAG	H362Q	XP_011514215.1

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