Product Details

SNP ID

rs150154487

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:104166859 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCGAGGAGCCCTTCCCACTCCTGG[C/G]ACCTCCTCGCGGGGTGGGCACCTGC

Phenotype

MIM: 300941

Polymorphism

C/G, 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	382	Missense Mutation	GCA,GGA	A25G	NP_997201.1
XM_005262079.2	382	Missense Mutation	GCA,GGA	A25G	XP_005262136.1
XM_017029270.1	382	Intron			XP_016884759.1

Gene

SLC25A53

Gene Name

solute carrier family 25 member 53

There are no transcripts associated with this gene.

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