Product Details

SNP ID

rs202239066

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:27100444 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGAAGACATCGTCGGTTCCTGGGG[A/G]CGAAGTCTCCTTGCTCCGCATCATG

Phenotype

MIM: 107310

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC9A1 PubMed Links

Gene Details

Gene

SLC9A1

Gene Name

solute carrier family 9 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003047.4	2185	Missense Mutation	CCC,TCC	P771S	NP_003038.2
XM_011542021.2	2185	Missense Mutation	CCC,TCC	P661S	XP_011540323.1

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