Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DNAJB9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249356
Start	108571832:108571832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106T>G
AA Mutation	p.Ser36Ala(p.S36A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249356
Start	108573203:108573203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522G>T
AA Mutation	p.Glu174Asp(p.E174D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000249356
Start	108573204:108573204(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.526delA
AA Mutation	p.Met176CysfsTer67(p.M176Cfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000249356
Start	108572949:108572949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268G>T
AA Mutation	p.Gly90Ter(p.G90*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000249356
Start	108571781:108571781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55G>T
AA Mutation	p.Glu19Ter(p.E19*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DNAJB9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249356
Start	108573307:108573307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748898841
CDS Mutation	c.626G>A
AA Mutation	p.Arg209Gln(p.R209Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249356
Start	108571833:108571833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762515467
CDS Mutation	c.107C>T
AA Mutation	p.Ser36Leu(p.S36L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249356
Start	108573265:108573265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584G>T
AA Mutation	p.Arg195Ile(p.R195I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript