Product Details

SNP ID

rs7882194

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.X:104157089 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACATTAACCGTTTCGCGACTACGTC[C/A]GTTGGCCGGTCTGTTTGGGAGAGCC

Phenotype

MIM: 300941

Polymorphism

C/A, 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	16	Intron			NP_997201.1
XM_005262079.2	16	Intron			XP_005262136.1
XM_017029270.1	16	UTR 5			XP_016884759.1

Gene

SLC25A53

Gene Name

solute carrier family 25 member 53

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012755.4	16	Intron			NP_001012773.2
XM_005262129.4	16	Intron			XP_005262186.1
XM_011530952.2	16	Intron			XP_011529254.1
XM_011530953.2	16	Intron			XP_011529255.1
XM_017029514.1	16	Intron			XP_016885003.1
XM_017029515.1	16	Intron			XP_016885004.1
XM_017029516.1	16	Intron			XP_016885005.1

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