Product Details

SNP ID: rs72647371
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:754129 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGGCGAGAAGTGGCAGCGGCGGCGG[C/T]AGCGCCAAGGAGCCACAGGAGGAAC
Phenotype: MIM: 605232
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: WNK1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184985.1	1532	Silent Mutation	GGC,GGT	G188G	NP_001171914.1
NM_014823.2	1532	Silent Mutation	GGC,GGT	G188G	NP_055638.2
NM_018979.3	1532	Silent Mutation	GGC,GGT	G188G	NP_061852.3
NM_213655.4	1532	Silent Mutation	GGC,GGT	G188G	NP_998820.3
XM_006719003.2	1532	Silent Mutation	GGC,GGT	G188G	XP_006719066.1
XM_011520997.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519299.1
XM_011520998.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519300.1
XM_011520999.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519301.1
XM_011521000.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519302.1
XM_011521001.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519303.1
XM_011521002.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519304.1
XM_011521003.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519305.1
XM_011521004.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519306.1
XM_011521005.2	1532	Intron			XP_011519307.1
XM_011521006.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519308.1
XM_011521007.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519309.1
XM_011521008.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519310.1
XM_011521009.2	1532	Silent Mutation	GGC,GGT	G188G	XP_011519311.1
XM_017019834.1	1532	Silent Mutation	GGC,GGT	G188G	XP_016875323.1
XM_017019835.1	1532	Silent Mutation	GGC,GGT	G188G	XP_016875324.1
XM_017019836.1	1532	Silent Mutation	GGC,GGT	G188G	XP_016875325.1
XM_017019837.1	1532	Silent Mutation	GGC,GGT	G188G	XP_016875326.1
XM_017019838.1	1532	Silent Mutation	GGC,GGT	G188G	XP_016875327.1
XM_017019839.1	1532	Silent Mutation	GGC,GGT	G188G	XP_016875328.1