Colon Cancer: Gene >> TM9SF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376387
Start	99554372:99554372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1557G>T
AA Mutation	p.Lys519Asn(p.K519N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376387
Start	99552274:99552274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436G>A
AA Mutation	p.Cys479Tyr(p.C479Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376387
Start	99520068:99520068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272G>A
AA Mutation	p.Arg91His(p.R91H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376387
Start	99543900:99543900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055A>G
AA Mutation	p.His352Arg(p.H352R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376387
Start	99539522:99539522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793A>G
AA Mutation	p.Ile265Val(p.I265V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376387
Start	99552222:99552222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1384T>C
AA Mutation	p.Ser462Pro(p.S462P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376387
Start	99554349:99554349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1534C>T
AA Mutation	p.Pro512Ser(p.P512S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376387
Start	99501755:99501755(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.155delA
AA Mutation	p.Lys52ArgfsTer9(p.K52Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376387
Start	99529560:99529560(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs753113250
CDS Mutation	c.433delA
AA Mutation	p.Ser145AlafsTer4(p.S145Afs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376387
Start	99501755:99501756(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.154_155delAA
AA Mutation	p.Lys52GlufsTer16(p.K52Efs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000376387
Start	99554322:99554322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507C>T
AA Mutation	p.Arg503Ter(p.R503*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TM9SF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376387
Start	99520068:99520068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272G>A
AA Mutation	p.Arg91His(p.R91H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376387
Start	99539554:99539554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376387
Start	99559395:99559395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs7330734
CDS Mutation	c.1785G>A
Mutation Classification	Silent
Feature Type	Transcript