Product Details

SNP ID

rs201163996

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:100573892 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGATCTTCTTCCTTTATGTTCCC[A/C]AAAACGCAGTCATCTTTAGCTATCT

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SNX31 PubMed Links

Gene Details

Gene

SNX31

Gene Name

sorting nexin 31

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152628.3	1527	Missense Mutation	TTG,TTT	L432F	NP_689841.3
XM_005250815.3	1527	Missense Mutation	TTG,TTT	L333F	XP_005250872.1
XM_011516899.1	1527	Missense Mutation	TTG,TTT	L366F	XP_011515201.1
XM_017013153.1	1527	Missense Mutation	TTG,TTT	L431F	XP_016868642.1
XM_017013154.1	1527	Missense Mutation	TTG,TTT	L431F	XP_016868643.1
XM_017013155.1	1527	Missense Mutation	TTG,TTT	L430F	XP_016868644.1
XM_017013156.1	1527	Missense Mutation	TTG,TTT	L413F	XP_016868645.1
XM_017013157.1	1527	Missense Mutation	TTG,TTT	L394F	XP_016868646.1
XM_017013158.1	1527	Missense Mutation	TTG,TTT	L393F	XP_016868647.1
XM_017013159.1	1527	Missense Mutation	TTG,TTT	L375F	XP_016868648.1
XM_017013160.1	1527	Missense Mutation	TTG,TTT	L364F	XP_016868649.1
XM_017013161.1	1527	Missense Mutation	TTG,TTT	L349F	XP_016868650.1
XM_017013162.1	1527	Missense Mutation	TTG,TTT	L326F	XP_016868651.1
XM_017013163.1	1527	Missense Mutation	TTG,TTT	L227F	XP_016868652.1
XM_017013164.1	1527	Intron			XP_016868653.1
XM_017013165.1	1527	Intron			XP_016868654.1

View Full Product Details