Colon Cancer: Gene >> WNK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	753879:753879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314C>A
AA Mutation	p.Pro105His(p.P105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	897532:897532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6299C>A
AA Mutation	p.Ser2100Tyr(p.S2100Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	861185:861185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1793C>T
AA Mutation	p.Ala598Val(p.A598V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	754272:754272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774337782
CDS Mutation	c.707A>T
AA Mutation	p.Tyr236Phe(p.Y236F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	885489:885489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4685C>A
AA Mutation	p.Ser1562Tyr(p.S1562Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	857165:857165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316T>C
AA Mutation	p.Val439Ala(p.V439A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	884864:884864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4060G>A
AA Mutation	p.Ala1354Thr(p.A1354T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	908631:908631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6988G>A
AA Mutation	p.Ala2330Thr(p.A2330T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	827092:827092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983G>A
AA Mutation	p.Cys328Tyr(p.C328Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	859358:859358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514G>A
AA Mutation	p.Arg505His(p.R505H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896592:896592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6105G>C
AA Mutation	p.Gln2035His(p.Q2035H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	885275:885275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4471T>C
AA Mutation	p.Ser1491Pro(p.S1491P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	885627:885627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781667314
CDS Mutation	c.4823C>T
AA Mutation	p.Ala1608Val(p.A1608V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	859391:859391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547A>G
AA Mutation	p.Tyr516Cys(p.Y516C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	885242:885242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4438G>A
AA Mutation	p.Ala1480Thr(p.A1480T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	900650:900650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6623G>A
AA Mutation	p.Ser2208Asn(p.S2208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	830117:830117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1268C>T
AA Mutation	p.Ser423Leu(p.S423L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	879907:879907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2708T>C
AA Mutation	p.Val903Ala(p.V903A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896393:896393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5906A>G
AA Mutation	p.Asp1969Gly(p.D1969G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	830151:830151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201053384
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	753574:753574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	879686:879686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2487G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	885493:885493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4689G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	827252:827252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1143G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	830145:830145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	859434:859434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1590A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	879593:879593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2394A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	885271:885271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4467A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315939
Start	813730:813733(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.849_852delTTAT
AA Mutation	p.Phe283LeufsTer8(p.F283Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000315939
Start	882961:882961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3391C>T
AA Mutation	p.Arg1131Ter(p.R1131*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315939
Start	753635:753636(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.75dupC
AA Mutation	p.Lys26GlnfsTer51(p.K26Qfs*51)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WNK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	859418:859418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1574C>A
AA Mutation	p.Ser525Tyr(p.S525Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896395:896395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5908A>C
AA Mutation	p.Thr1970Pro(p.T1970P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	827131:827131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341Gln(p.R341Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	894568:894568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5516A>C
AA Mutation	p.Gln1839Pro(p.Q1839P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896689:896689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6202G>A
AA Mutation	p.Glu2068Lys(p.E2068K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript