Product Details

SNP ID

rs75871344

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:93184958 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACGGCGATGGCGGCCGCCGAGACG[G/T]CCCCGGCACGCTGATGGAGCCCGGG

Phenotype

MIM: 606249

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

WNK2 PubMed Links

Gene Details

Gene

WNK2

Gene Name

WNK lysine deficient protein kinase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282394.1	261	Missense Mutation	GGC,GTC	G10V	NP_001269323.1
NM_006648.3	261	Missense Mutation	GGC,GTC	G10V	NP_006639.3
XM_005252137.3	261	Missense Mutation	GGC,GTC	G10V	XP_005252194.1
XM_005252140.2	261	Missense Mutation	GGC,GTC	G10V	XP_005252197.1
XM_005252141.2	261	Missense Mutation	GGC,GTC	G10V	XP_005252198.1
XM_005252144.2	261	Missense Mutation	GGC,GTC	G10V	XP_005252201.1
XM_011518926.2	261	Missense Mutation	GGC,GTC	G10V	XP_011517228.1
XM_011518927.2	261	Missense Mutation	GGC,GTC	G10V	XP_011517229.1
XM_011518928.2	261	Missense Mutation	GGC,GTC	G10V	XP_011517230.1
XM_011518929.2	261	Missense Mutation	GGC,GTC	G10V	XP_011517231.1
XM_011518930.2	261	Missense Mutation	GGC,GTC	G10V	XP_011517232.1
XM_011518931.2	261	Missense Mutation	GGC,GTC	G10V	XP_011517233.1
XM_011518932.2	261	Missense Mutation	GGC,GTC	G10V	XP_011517234.1
XM_011518935.2	261	Missense Mutation	GGC,GTC	G10V	XP_011517237.1
XM_011518936.2	261	Missense Mutation	GGC,GTC	G10V	XP_011517238.1
XM_011518937.2	261	Intron			XP_011517239.1
XM_011518939.2	261	Intron			XP_011517241.1
XM_011518940.2	261	Intron			XP_011517242.1
XM_017015045.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870534.1
XM_017015046.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870535.1
XM_017015047.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870536.1
XM_017015048.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870537.1
XM_017015049.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870538.1
XM_017015050.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870539.1
XM_017015051.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870540.1
XM_017015052.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870541.1
XM_017015053.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870542.1
XM_017015054.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870543.1
XM_017015055.1	261	Missense Mutation	GGC,GTC	G10V	XP_016870544.1

View Full Product Details