Colon Cancer: Gene >> TRAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3658831:3658831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764916149
CDS Mutation	c.1975G>A
AA Mutation	p.Ala659Thr(p.A659T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3676045:3676045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376597215
CDS Mutation	c.805C>T
AA Mutation	p.Arg269Trp(p.R269W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3671759:3671759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1198C>A
AA Mutation	p.Leu400Ile(p.L400I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3675371:3675371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757572551
CDS Mutation	c.841G>A
AA Mutation	p.Val281Ile(p.V281I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3664386:3664386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1457A>G
AA Mutation	p.Tyr486Cys(p.Y486C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3658834:3658834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139636268
CDS Mutation	c.1972C>T
AA Mutation	p.Arg658Cys(p.R658C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3663477:3663477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765500192
CDS Mutation	c.1655C>T
AA Mutation	p.Thr552Met(p.T552M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3664360:3664360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113510154
CDS Mutation	c.1483C>T
AA Mutation	p.Arg495Cys(p.R495C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3686084:3686084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61758086
CDS Mutation	c.383G>A
AA Mutation	p.Arg128His(p.R128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3686082:3686082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385C>T
AA Mutation	p.His129Tyr(p.H129Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3664428:3664428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1415C>T
AA Mutation	p.Ser472Phe(p.S472F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3674365:3674365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775599442
CDS Mutation	c.1018C>T
AA Mutation	p.Arg340Cys(p.R340C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3674426:3674426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3658853:3658853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756385239
CDS Mutation	c.1953C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3676100:3676100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246957
Start	3666038:3666039(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1315_1316delAA
AA Mutation	p.Lys439ValfsTer3(p.K439Vfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000246957
Start	3674449:3674449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>T
AA Mutation	p.Glu312Ter(p.E312*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3675336:3675336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.876G>T
AA Mutation	p.Met292Ile(p.M292I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3675372:3675372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377042927
CDS Mutation	c.840C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246957
Start	3666057:3666058(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1296dupA
AA Mutation	p.Asp433ArgfsTer3(p.D433Rfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript