Colon Cancer: Gene >> DNAJB8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319153
Start	128463126:128463126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120G>T
AA Mutation	p.Glu40Asp(p.E40D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319153
Start	128462582:128462582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529782278
CDS Mutation	c.664G>A
AA Mutation	p.Gly222Ser(p.G222S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319153
Start	128462614:128462614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632A>G
AA Mutation	p.Glu211Gly(p.E211G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319153
Start	128462674:128462674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373509985
CDS Mutation	c.572G>A
AA Mutation	p.Gly191Asp(p.G191D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319153
Start	128462821:128462821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425C>T
AA Mutation	p.Pro142Leu(p.P142L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319153
Start	128463175:128463175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140964428
CDS Mutation	c.71G>A
AA Mutation	p.Arg24His(p.R24H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319153
Start	128463220:128463220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26G>A
AA Mutation	p.Gly9Asp(p.G9D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319153
Start	128463207:128463207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319153
Start	128462715:128462715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370646538
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319153
Start	128462763:128462763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DNAJB8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319153
Start	128462596:128462596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200292314
CDS Mutation	c.650C>T
AA Mutation	p.Ser217Leu(p.S217L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript