Product Details

SNP ID

rs61734269

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:49812948 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGGGGGAGAAGATGGCGGAAGAGG[A/C]GTGAGTGGGCTTTTTCCCGGGCGGC

Phenotype

MIM: 612730

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC9A8 PubMed Links

Gene Details

Gene

SLC9A8

Gene Name

solute carrier family 9 member A8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001260491.1	98	Missense Mutation	GAG,GCG	E9A	NP_001247420.1
NM_015266.2	98	Missense Mutation	GAG,GCG	E9A	NP_056081.1
XM_006723756.1	98	Missense Mutation	GAG,GCG	E9A	XP_006723819.1
XM_011528736.1	98	Missense Mutation	GAG,GCG	E9A	XP_011527038.1
XM_011528737.1	98	Missense Mutation	GAG,GCG	E9A	XP_011527039.1
XM_011528738.1	98	Missense Mutation	GAG,GCG	E9A	XP_011527040.1
XM_011528739.1	98	Missense Mutation	GAG,GCG	E9A	XP_011527041.1
XM_011528740.1	98	Missense Mutation	GAG,GCG	E9A	XP_011527042.1
XM_011528741.1	98	Missense Mutation	GAG,GCG	E9A	XP_011527043.1
XM_011528742.1	98	UTR 5			XP_011527044.1
XM_011528743.2	98	Intron			XP_011527045.1
XM_011528744.2	98	Intron			XP_011527046.1
XM_011528745.1	98	Missense Mutation	GAG,GCG	E9A	XP_011527047.1
XM_017027754.1	98	Missense Mutation	GAG,GCG	E9A	XP_016883243.1
XM_017027755.1	98	UTR 5			XP_016883244.1
XM_017027756.1	98	UTR 5			XP_016883245.1

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