Product Details

SNP ID

rs200779428

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:104186104 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACATTGCCAGTGGGAGTGATGTACT[G/T]TCTGATGTCATACCCAGTATTCCAA

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

FAM199X PubMed Links

Gene Details

Gene

FAM199X

Gene Name

family with sequence similarity 199, X-linked

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207318.3	764	Silent Mutation	CTG,CTT	L152L	NP_997201.1
XM_005262079.2	764	Silent Mutation	CTG,CTT	L152L	XP_005262136.1
XM_017029270.1	764	UTR 5			XP_016884759.1

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