Colon Cancer: Gene >> KHDRBS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355849
Start	135647044:135647044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001C>A
AA Mutation	p.Ala334Glu(p.A334E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355849
Start	135557536:135557536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376433950
CDS Mutation	c.560G>A
AA Mutation	p.Arg187Gln(p.R187Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355849
Start	135548782:135548782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779240853
CDS Mutation	c.353C>T
AA Mutation	p.Ala118Val(p.A118V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355849
Start	135548854:135548854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425C>T
AA Mutation	p.Ala142Val(p.A142V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355849
Start	135521288:135521288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140A>T
AA Mutation	p.Asp47Val(p.D47V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355849
Start	135607013:135607013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866A>G
AA Mutation	p.Asn289Ser(p.N289S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355849
Start	135647007:135647007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964A>G
AA Mutation	p.Thr322Ala(p.T322A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355849
Start	135647063:135647063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355849
Start	135582049:135582049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577272565
CDS Mutation	c.783G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355849
Start	135606981:135606981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.834T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000355849
Start	135557535:135557535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Ter(p.R187*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355849
Start	135542672:135542673(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.230dupT
AA Mutation	p.Leu77PhefsTer49(p.L77Ffs*49)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KHDRBS3

No Mutation Annotation!