Colon Cancer: Gene >> TRAIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331456
Start	49832016:49832016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937G>T
AA Mutation	p.Asp313Tyr(p.D313Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331456
Start	49843896:49843896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313G>A
AA Mutation	p.Asp105Asn(p.D105N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331456
Start	49831971:49831971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756941913
CDS Mutation	c.982C>T
AA Mutation	p.Arg328Trp(p.R328W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331456
Start	49840322:49840322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757G>T
AA Mutation	p.Ala253Ser(p.A253S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331456
Start	49830022:49830022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1084A>G
AA Mutation	p.Lys362Glu(p.K362E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331456
Start	49830024:49830024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082G>T
AA Mutation	p.Arg361Met(p.R361M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331456
Start	49848182:49848182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.117G>T
AA Mutation	p.Glu39Asp(p.E39D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331456
Start	49829206:49829206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148292576
CDS Mutation	c.1307G>A
AA Mutation	p.Arg436His(p.R436H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331456
Start	49832033:49832033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767904431
CDS Mutation	c.920G>A
AA Mutation	p.Arg307Gln(p.R307Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331456
Start	49843825:49843825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149686258
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331456
Start	49841903:49841903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331456
Start	49829157:49829157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1356G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331456
Start	49829689:49829689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1164delT
AA Mutation	p.Phe388LeufsTer7(p.F388Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000331456
Start	49848142:49848142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TRAIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331456
Start	49829160:49829160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353G>T
AA Mutation	p.Arg451Ser(p.R451S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript