Product Details

SNP ID

rs138809007

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:9295976 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAAAGGTCTTCCCACACTCCTTACA[G/T]TCATACTGTATCTTTCCAGTGTGAT

Phenotype

MIM: 609571

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ZNF699 PubMed Links

Gene Details

Gene

ZNF699

Gene Name

zinc finger protein 699

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198535.2	1798	Missense Mutation	GAA,GAC	E476D	NP_940937.1

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