Product Details

SNP ID

rs6621790

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:104180338 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTACAGACTTTGTATTTAAAATCA[A/G]ACTACAAGGATTCTTAGTAAAGCAT

Phenotype

Polymorphism

A/G, Transition 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		Intron			NP_997201.1
XM_005262079.2		Intron			XP_005262136.1
XM_017029270.1		Intron			XP_016884759.1

View Full Product Details