Product Details

SNP ID

rs187969464

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:99546804 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTATTTCTCTTCTTTGTTTTTAAC[A/C]GTGTCAAGATTGAAAATCCTAGTTC

Phenotype

Polymorphism

A/C, 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	1788	Missense Mutation			NP_659802.1
XM_011515911.2	1788	Missense Mutation			XP_011514213.1
XM_011515913.2	1788	Missense Mutation			XP_011514215.1

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