All variants in the STK11 gene

Information The variants shown are described using the NM_000455.4 transcript reference sequence.

536 entries on 6 pages. Showing entries 1 - 100.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Type     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Variant remarks     

ClassClinical     

Owner     
./. 00 c.-1795T>C - - - - GenBank STK11_00408 - - - Qi Ming
./. 00 c.-1494A>C - - - - GenBank STK11_00410 - - - Qi Ming
./. 01 c.-1115-u161G>T - = c.-1275G/T - GenBank STK11_00394 - A SNP site, its function remain to be seen. - Qi Ming
./. 01 c. -1115_290+?del - - exon 1 was deleted - GenBank STK11_00412 - - - Qi Ming
./. 01 c.-1114_290+1del - ? Exon 1 deleted - GenBank STK11_00462 - male,Clinical presentation:Buccal freckling, polyps male,Clinical presentation:Multiple polyps female,Clinical presentation:Multiple polyps, buccal freckling - Qi Ming
./. 01 c.-1114-?_291+?del - p.? Promoter and Exon 1 deletion - GenBank STK11_00468 - - - Qi Ming
./. 01 c.-1114-?_291+?del - p.? Promoter and Exon 1 deletion - GenBank STK11_00468 - - - Qi Ming
./. 01 c.-1114-?_862+?del - p.? Promoter to Exon 6 deletion - GenBank STK11_00474 - - - Qi Ming
./. 01 c.-458G>C - - - - GenBank STK11_00411 - - - Qi Ming
./. 01 c.-160G>T - - - - GenBank STK11_00409 - - - Qi Ming
./. 04 ? - - IVS4+193 G>C - GenBank STK11_00275 - male,Clinical presentation:Intussusception - Qi Ming
./. 03 ? - p.Gln152fsX160 p.Q152fsX160 - GenBank STK11_00275 - - - Qi Ming
./. 03 ? - p.Gln152fsX161 p.Q152fsX161 - GenBank STK11_00275 - - - Qi Ming
./. 03 ? - p.Leu140fsX160 p.L140fsX160 - GenBank STK11_00275 - - - Qi Ming
./. 04 ? - p.Leu164fsX287 p.L164fsX287 - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - p.Leu263fsX286 p.L263fsX286 - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - p.Leu282fsX284 p.L282fsX284 - GenBank STK11_00275 - - - Qi Ming
./. 03 ? - p.Val142fsX162 p.V142fsX162 - GenBank STK11_00275 - - - Qi Ming
./. 04 ? - p.Val168fsX283 p.V168fsX283 - GenBank STK11_00275 - - - Qi Ming
./. 04 ? - p.Phe157fsX160 p.F157fsX160 - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - p.Phe264fsX285 p.F264fsX285 - GenBank STK11_00275 - - - Qi Ming
./. 04 ? - p.Ile172fsX265 p.I172fsX265 - GenBank STK11_00275 - - - Qi Ming
./. 04 ? - p.Asp179fsX265 p.D179fsX265 - GenBank STK11_00275 - - - Qi Ming
./. 08 ? - p.Asp327fsX359 p.D327fsX359 - GenBank STK11_00275 - - - Qi Ming
./. 04 ? - p.Gly196fsX265 p.G196fsX265 - GenBank STK11_00275 - - - Qi Ming
./. 05 ? - p.Gly215fsX286 p.G215fsX286 - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - p.Gly251fsX286 p.G251fsX286 - GenBank STK11_00275 - - - Qi Ming
./. 05 ? - p.Pro203fsX287 p.P203fsX287 - GenBank STK11_00275 - - - Qi Ming
./. 05 ? - p.Pro222fsX286 p.P222fsX286 - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - p.Pro281fsX286 p.P281fsX286 - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - p.Pro281fsX284 p.P281fsX284 - GenBank STK11_00275 - - - Qi Ming
./. 08 ? - p.Pro319fsX335 p.P319fsX335 - GenBank STK11_00275 - - - Qi Ming
./. 08 ? - p.Pro324fsX357 p.P324fsX357 - GenBank STK11_00275 - - - Qi Ming
./. 05 ? - p.Thr212fsX263 p.T212fsX263 - GenBank STK11_00275 - - - Qi Ming
./. 05 ? - p.Trp239fsX285 p.W239fsX285 - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - p.Lys287fsX331 p.K287fsX331 - GenBank STK11_00275 - - - Qi Ming
./. 07 ? - p.Arg304fsX335 p.R304fsX335 - GenBank STK11_00275 - - - Qi Ming
./. ? ? - - Genomic deletion - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - - IVS5del52 - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - - IVS5del52 - GenBank STK11_00275 - - - Qi Ming
./. 06 ? - - IVS6del52 - GenBank STK11_00275 - - - Qi Ming
./. 04 ? - - IVS4del14 - GenBank STK11_00275 - - - Qi Ming
./. ? ? - - Whole gene deletion - GenBank STK11_00275 - - - Qi Ming
./. ? ? - - Promoter and exon 1 deletion - GenBank STK11_00275 - - - Qi Ming
./. ? ? - - Promoter deletion - GenBank STK11_00275 - - - Qi Ming
./. ? ? - - Promoter and exon 1 - GenBank STK11_00275 - - - Qi Ming
./. 08 c.? - p.? codon 307 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - - 55 - GenBank STK11_00047 - - - Qi Ming
./. 06 c.? - - 277 - GenBank STK11_00044 - - - Qi Ming
./. 04 c.? - - codons156_307 deleted - GenBank STK11_00037 - inv/del exons4 to 7 - Qi Ming
./. 04 c.? - - G2412A codon156 - GenBank STK11_00037 - splice acceptor defect exon4 skipping;stop at codon242 - Qi Ming
./. 05 c.? - p.? Exon 5 245 1-bp (C) deletion - GenBank STK11_00052 - Frameshift; stop at codon 286 - Qi Ming
./. 06 c.? - p.? Exon 6 281 1-bp (C) deletion - GenBank STK11_00055 - - - Qi Ming
./. 06 c.? - p.? Exon 6 281 1-bp (C) insertion - GenBank STK11_00048 - - - Qi Ming
./. 01 c.? - p.? Exon 1 codon 38 2-bp (GC) insertion - GenBank STK11_00037 - Frameshift; stop at codon 51 - Qi Ming
./. 06 c.? - p.? Exon 6 codon 281 1-bp (C) insertion - GenBank STK11_00037 - Frameshift; stop at codon 284 - Qi Ming
./. 01 c.? - p.? 150 - GenBank STK11_00073 - - - Qi Ming
./. 04 c.? - - Codon189 - GenBank STK11_00037 - - - Qi Ming
./. 05 c.? - p? 5 214 - GenBank STK11_00037 - - - Qi Ming
./. 05 c.? - p.? 5 216 - GenBank STK11_00037 - - - Qi Ming
./. 06 c.? - - Exon6 280 C insertion - GenBank STK11_00177 - Frameshift, stop at codon 284 - Qi Ming
./. 06 c.? - ? 3256C>G - GenBank STK11_00236 - This nucleotide substitution cause s a premature stop codon, Tyr246X, presumablyresulting in a truncated protein. - Qi Ming
./. 06 c.? - - c.852T>C - GenBank STK11_00037 - male,Clinical presentation:Intussusception - Qi Ming
./. 01 c.? - p.Met18fsX162 p.M18fsX162 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.Met51fsX162 p.M51fsX162 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.Asp53fsX64 p.D53fsX64 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.GlufsX63 p.E57fsX63 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.Glu58fsX161 p.E58fsX161 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.Tyr80fsX161 p.Y80fsX161 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.Tyr80fsX162 p.Y80fsX162 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.Val88fsX152 p.V88fsX152 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.Lys97fsX103 p.K97fsX103 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.Lys97fsX103 p.K97fsX103 - GenBank STK11_00037 - - - Qi Ming
./. 02 c.? - p.Gln112fsX118 p.Q112fsX128 - GenBank STK11_00037 - - - Qi Ming
./. 02 c.? - p.Val116fsX163 p.V116fsX163 - GenBank STK11_00037 - - - Qi Ming
./. 02 c.? - p.Gln123fsX128 p.Q123fsX128 - GenBank STK11_00037 - - - Qi Ming
./. 06 c.? - p.Phe264fsX284 p.F264fsX284 - GenBank STK11_00037 - - - Qi Ming
./. 06 c.? - p.Ile248fsX268 p.I248fsX268 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - - del5`UTR+exon1 - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p? 150_151ins6 - GenBank STK11_00037 - - - Qi Ming
./. 07 c.? - p.? IVS6&Ex7; del52 - GenBank STK11_00037 - Abnormal splicing;truncated protein - Qi Ming
./. 04 c.? - p.? Intron 3& Exon 4:2407_2413delCGCAGGinsTGCAC - GenBank STK11_00037 - - - Qi Ming
./. 04 c.? - p.? Intron 3& Exon 4;2412_2413delGGinsC - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.? c.1-?_290+?del - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.? c.1-?_464+?del - GenBank STK11_00037 - - - Qi Ming
./. 01 c.? - p.? c.1-?_920+?del - GenBank STK11_00037 - - - Qi Ming
./. 00 c.? - p.? Whole gene deletion - GenBank STK11_00037 - - - Qi Ming
./. 00 c.? - p.? Whole gene deletion - GenBank STK11_00037 - - - Qi Ming
./. ? c.1_464del - ? Exon 1_3 deleted - GenBank STK11_00280 - male,Clinical presentation:Intussusception - Qi Ming
./. 01 c.40G>A - p.Glu14Lys - - GenBank STK11_00363 - - - Qi Ming
./. 01 c.95C>G - p.Thr32Ser - - GenBank STK11_00395 - - - Qi Ming
./. 01 c.96C>G - p.Thr32Thr - - GenBank STK11_00422 - If the STK11 gene is one of the mutational targets of microsatellite instability, its inactivation may be associated with tumor development in a small proportion of colorectal cancers. - Qi Ming
./. 01 c. 108C>A - p.Tyr36X Codon 36 Exon 1 TAC CAG toTAA CAG - GenBank STK11_00330 - - - Qi Ming
./. 01 c. 109C>T - p.Gln37X Q37X - GenBank STK11_00288 - - - Qi Ming
./. 01 c.109C>T - p.Gln37X - - GenBank STK11_00348 - A549 cell line. - Qi Ming
./. 01 c.109C>T - p.Gln37X - - GenBank STK11_00348 - - - Qi Ming
./. 01 c.109C>T - p.Gln37X - - GenBank STK11_00348 - Point mutation in STK11 may be chief in Chinese with PJS and the frequency of mutation was fewer than that in previous reports. It suggested that there may be genetic heterogeneity in PJS. - Qi Ming
./. 01 c.111delG - p.Gln37HisfsX14 Codon37 G deletion - GenBank STK11_00169 - - - Qi Ming
./. 01 c.115_125delCGCCGCAAGCG - p.Arg39GlyfsX120 c.115_125delCGCCGCAAGCG - GenBank STK11_00239 - - - Qi Ming
./. 01 c.116_117insGC - p.Arg40ProfsX12 455_456insGC - GenBank STK11_00078 - - - Qi Ming
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