Colon Cancer: Gene >> WFS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6301728:6301728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1933C>A
AA Mutation	p.Leu645Met(p.L645M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6300693:6300693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754391419
CDS Mutation	c.898A>G
AA Mutation	p.Lys300Glu(p.K300E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6302232:6302232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756972444
CDS Mutation	c.2437G>A
AA Mutation	p.Val813Met(p.V813M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6301720:6301720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1925C>T
AA Mutation	p.Ala642Val(p.A642V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6302460:6302460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2665G>A
AA Mutation	p.Ala889Thr(p.A889T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6289126:6289126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455G>A
AA Mutation	p.Arg152Lys(p.R152K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6295181:6295181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853C>T
AA Mutation	p.Arg285Cys(p.R285C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6291979:6291979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Cys(p.R232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6301161:6301161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144452795
CDS Mutation	c.1366C>T
AA Mutation	p.Arg456Cys(p.R456C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6289072:6289072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746010848
CDS Mutation	c.401C>T
AA Mutation	p.Ala134Val(p.A134V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226760
Start	6300986:6300986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201394228
CDS Mutation	c.1191C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226760
Start	6277539:6277539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226760
Start	6301913:6301913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375408391
CDS Mutation	c.2118C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226760
Start	6289022:6289022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200831572
CDS Mutation	c.351G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226760
Start	6291939:6291939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs727504666
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226760
Start	6302000:6302000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs71530911
CDS Mutation	c.2205C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226760
Start	6300668:6300668(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.877delC
AA Mutation	p.Leu293CysfsTer11(p.L293Cfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> WFS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226760
Start	6302011:6302011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2216A>G
AA Mutation	p.Tyr739Cys(p.Y739C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript