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 |
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