Transcript #00011331

Transcript name transcript variant 1
Gene name WNK1 (WNK lysine deficient protein kinase 1)
Chromosome 12
Transcript - NCBI ID NM_018979.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_061852.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

124 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-91T>G r.(=) p.(=)
./. - c.-25C>G r.(=) p.(=)
./. - c.-20C>T r.(=) p.(=)
./. - c.48G>T r.(=) p.(=)
./. - c.192C>T r.(=) p.(=)
./. - c.258T>C r.(=) p.(=)
./. - c.421G>A r.(?) p.(Ala141Thr)
./. - c.446C>T r.(?) p.(Ala149Val)
./. - c.684C>T r.(=) p.(=)
./. - c.759+15A>C r.(=) p.(=)
./. - c.759+15_759+16insCTT r.(=) p.(=)
./. - c.759+27G>A r.(=) p.(=)
./. - c.759+101G>A r.(=) p.(=)
./. - c.759+120A>T r.(=) p.(=)
./. - c.1074C>T r.(=) p.(=)
./. - c.1153+40C>G r.(=) p.(=)
./. - c.1287A>G r.(=) p.(=)
./. - c.1312-119G>A r.(=) p.(=)
./. - c.1312-113_1312-112insA r.(=) p.(=)
./. - c.1400+44A>G r.(=) p.(=)
./. - c.1401-11C>A r.(=) p.(=)
./. - c.1479T>C r.(=) p.(=)
./. - c.1512A>G r.(=) p.(=)
./. - c.1526T>C r.(?) p.(Ile509Thr)
./. - c.1621-85del r.(=) p.(=)
./. - c.1621-71C>T r.(=) p.(=)
./. - c.1621-52G>T r.(=) p.(=)
./. - c.1739del r.(?) p.(Lys583Serfs*11)
./. - c.1759A>G r.(?) p.(Ser587Gly)
./. - c.1855A>G r.(?) p.(Thr619Ala)
./. - c.1994C>T r.(?) p.(Thr665Ile)
./. - c.2081T>C r.(?) p.(Ile694Thr)
./. - c.2139+2701_2139+2702insA r.(=) p.(=)
./. - c.2139+2855A>G r.(=) p.(=)
./. - c.2139+2872T>C r.(=) p.(=)
./. - c.2139+2872_2139+2873insC r.(=) p.(=)
./. - c.2139+2890G>C r.(=) p.(=)
./. - c.2139+2919_2139+2920insC r.(=) p.(=)
./. - c.2139+2966C>T r.(=) p.(=)
./. - c.2139+2968T>C r.(=) p.(=)
./. - c.2139+3014T>C r.(=) p.(=)
./. - c.2139+3063G>A r.(=) p.(=)
./. - c.2140-3496C>T r.(=) p.(=)
./. - c.2140-3343A>G r.(=) p.(=)
./. - c.2140-2855G>T r.(=) p.(=)
./. - c.2206A>G r.(?) p.(Ile736Val)
./. - c.2328G>A r.(=) p.(=)
./. - c.2373+7del r.(=) p.(=)
./. - c.2373+7dup r.(=) p.(=)
./. - c.2373+7_2373+8insTT r.(=) p.(=)
./. - c.2373+22A>T r.(=) p.(=)
./. - c.2490G>A r.(=) p.(=)
./. - c.2529G>A r.(=) p.(=)
./. - c.2832+40G>C r.(=) p.(=)
./. - c.2833-72del r.(=) p.(=)
./. - c.2833-72G>T r.(=) p.(=)
./. - c.2833-68G>T r.(=) p.(=)
./. - c.2833-66C>T r.(=) p.(=)
./. - c.2833-48T>C r.(=) p.(=)
./. - c.2898G>A r.(=) p.(=)
./. - c.3112-10C>T r.(=) p.(=)
./. - c.3166A>C r.(?) p.(Thr1056Pro)
./. - c.3209+44C>T r.(=) p.(=)
./. - c.3209+54C>T r.(=) p.(=)
./. - c.3292A>G r.(?) p.(Thr1098Ala)
./. - c.3489+4C>T r.spl? p.?
./. - c.3489+120A>T r.(=) p.(=)
./. - c.3490-5T>A r.spl? p.?
./. - c.3578G>A r.(?) p.(Ser1193Asn)
./. - c.3582G>A r.(=) p.(=)
./. - c.3654A>G r.(=) p.(=)
./. - c.3659C>T r.(?) p.(Ser1220Phe)
./. - c.3663+35_3663+36insT r.(=) p.(=)
./. - c.3664-15T>A r.(=) p.(=)
./. - c.3721+64G>A r.(=) p.(=)
./. - c.3844+42G>T r.(=) p.(=)
./. - c.3845-65A>G r.(=) p.(=)
./. - c.3960C>T r.(=) p.(=)
./. - c.4044C>T r.(=) p.(=)
./. - c.4517G>C r.(?) p.(Cys1506Ser)
./. - c.4603_4605del r.(?) p.(Ser1536del)
./. - c.5280+41_5280+42insT r.(=) p.(=)
./. - c.5281-30C>T r.(=) p.(=)
./. - c.5281-4G>A r.spl? p.?
./. - c.5365-82A>T r.(=) p.(=)
./. - c.5365-34C>T r.(=) p.(=)
./. - c.5397A>G r.(=) p.(=)
./. - c.5424G>T r.(?) p.(Met1808Ile)
./. - c.5449-121G>A r.(=) p.(=)
./. - c.5449-90T>G r.(=) p.(=)
./. - c.5451T>G r.(=) p.(=)
./. - c.5468C>T r.(?) p.(Pro1823Leu)
./. - c.5481A>G r.(=) p.(=)
./. - c.5509+83A>G r.(=) p.(=)
./. - c.5509+166G>A r.(=) p.(=)
./. - c.5583+3A>G r.spl? p.?
./. - c.5583+36C>T r.(=) p.(=)
./. - c.5584-75T>C r.(=) p.(=)
./. - c.5693G>C r.(?) p.(Ser1898Thr)
./. - c.5991G>A r.(=) p.(=)
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