Colon Cancer: Gene >> DKC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369550
Start	154768424:154768424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.763A>G
AA Mutation	p.Ser255Gly(p.S255G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369550
Start	154773200:154773200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1106T>C
AA Mutation	p.Val369Ala(p.V369A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369550
Start	154764937:154764937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782010351
CDS Mutation	c.55C>T
AA Mutation	p.Arg19Trp(p.R19W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369550
Start	154765448:154765448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89T>C
AA Mutation	p.Ile30Thr(p.I30T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369550
Start	154769242:154769242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Trp(p.R283W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369550
Start	154775269:154775269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782117503
CDS Mutation	c.1334C>T
AA Mutation	p.Ala445Val(p.A445V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369550
Start	154776241:154776241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1393T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369550
Start	154773168:154773168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781915787
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369550
Start	154775252:154775252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143207180
CDS Mutation	c.1317C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DKC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369550
Start	154775266:154775266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1331C>T
AA Mutation	p.Thr444Ile(p.T444I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript