Product Details

SNP ID

rs4947106

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:111100163 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTAAACTTTAGATTAGTCTATTTA[C/T]GGGTCACCTGGAAGATTCTTTATAA

Phenotype

MIM: 607550

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC16A10 PubMed Links

Gene Details

Gene

SLC16A10

Gene Name

solute carrier family 16 member 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018593.4		Intron			NP_061063.2
XM_006715329.2		Intron			XP_006715392.1
XM_011535422.2		Intron			XP_011533724.1
XM_017010237.1		Intron			XP_016865726.1

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