Product Details

SNP ID

rs139160191

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:34567984 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTATTAGCATTTTCATAATCCAC[C/T]AGTGACCTAGACCTTCGATACAGGA

Phenotype

MIM: 606098

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SNX6 PubMed Links

Gene Details

Gene

SNX6

Gene Name

sorting nexin 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021249.3	1100	Silent Mutation	CTA,CTG	L201L	NP_067072.3
NM_152233.2	1100	Silent Mutation	CTA,CTG	L329L	NP_689419.2
XM_006720224.1	1100	Silent Mutation	CTA,CTG	L292L	XP_006720287.1

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