Colon Cancer: Gene >> DDX3X

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399959
Start	41346908:41346908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1665T>G
AA Mutation	p.Asp555Glu(p.D555E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399959
Start	41346547:41346547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1540A>G
AA Mutation	p.Ile514Val(p.I514V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399959
Start	41346393:41346393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1480A>C
AA Mutation	p.Ile494Leu(p.I494L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399959
Start	41342572:41342572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>A
AA Mutation	p.Arg121His(p.R121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399959
Start	41343296:41343296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624G>C
AA Mutation	p.Lys208Asn(p.K208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399959
Start	41342547:41342547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337A>G
AA Mutation	p.Arg113Gly(p.R113G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399959
Start	41347648:41347648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1918G>A
AA Mutation	p.Gly640Arg(p.G640R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399959
Start	41342522:41342522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750187385
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000399959
Start	41345503:41345503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1270G>T
AA Mutation	p.Glu424Ter(p.E424*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399959
Start	41347649:41347650(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1919_1920insTGCTGAACTTA
AA Mutation	p.Gly641AlafsTer32(p.G641Afs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DDX3X

No Mutation Annotation!