Colon Cancer: Gene >> WNK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42787799:42787799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1763A>C
AA Mutation	p.Tyr588Ser(p.Y588S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42783954:42783954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809G>A
AA Mutation	p.Arg270Gln(p.R270Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42795823:42795823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3221A>G
AA Mutation	p.Asp1074Gly(p.D1074G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42796027:42796027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369907969
CDS Mutation	c.3425G>A
AA Mutation	p.Arg1142Gln(p.R1142Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42785450:42785450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs387907556
CDS Mutation	c.1444C>T
AA Mutation	p.Arg482Trp(p.R482W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42795119:42795119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2698A>G
AA Mutation	p.Thr900Ala(p.T900A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42787410:42787410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1609C>T
AA Mutation	p.Pro537Ser(p.P537S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42787333:42787333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779595489
CDS Mutation	c.1532G>A
AA Mutation	p.Arg511His(p.R511H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42794633:42794633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2315C>A
AA Mutation	p.Pro772His(p.P772H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000246914
Start	42781295:42781295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597G>T
AA Mutation	p.Glu199Asp(p.E199D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246914
Start	42781073:42781073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246914
Start	42784060:42784060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246914
Start	42784537:42784537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763075218
CDS Mutation	c.1128C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246914
Start	42781175:42781175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246914
Start	42782856:42782856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246914
Start	42782922:42782922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371430478
CDS Mutation	c.783G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246914
Start	42788172:42788173(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1908_1909delTT
AA Mutation	p.Ser637ProfsTer14(p.S637Pfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246914
Start	42794646:42794646(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2332delC
AA Mutation	p.Leu778SerfsTer157(p.L778Sfs*157)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246914
Start	42787852:42787852(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762079039
CDS Mutation	c.1822delG
AA Mutation	p.Val608CysfsTer53(p.V608Cfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246914
Start	42785399:42785399(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1398delG
AA Mutation	p.Arg467AlafsTer194(p.R467Afs*194)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246914
Start	42796545:42796545(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3700delG
AA Mutation	p.Val1234Ter(p.V1234*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> WNK4

No Mutation Annotation!