Colon Cancer: Gene >> TNFAIP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137871495:137871495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747030410
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Trp(p.R90W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137879141:137879141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696G>T
AA Mutation	p.Asp566Tyr(p.D566Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137880198:137880198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2034C>A
AA Mutation	p.Phe678Leu(p.F678L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137871444:137871444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217A>G
AA Mutation	p.Ile73Val(p.I73V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137879316:137879316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1871G>A
AA Mutation	p.Cys624Tyr(p.C624Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137875719:137875719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518A>C
AA Mutation	p.Lys173Thr(p.K173T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137878688:137878688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243C>A
AA Mutation	p.Gln415Lys(p.Q415K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137871435:137871435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375335818
CDS Mutation	c.208G>A
AA Mutation	p.Asp70Asn(p.D70N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237289
Start	137880129:137880129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1965T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237289
Start	137878612:137878612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781274783
CDS Mutation	c.1167G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000237289
Start	137878808:137878808(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1368delG
AA Mutation	p.Pro457LeufsTer20(p.P457Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000237289
Start	137878807:137878808(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1368dupG
AA Mutation	p.Pro457AlafsTer16(p.P457Afs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TNFAIP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137881242:137881242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs5029957
CDS Mutation	c.2296G>A
AA Mutation	p.Ala766Thr(p.A766T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137881287:137881287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2341G>A
AA Mutation	p.Glu781Lys(p.E781K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000237289
Start	137874956:137874956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407G>A
AA Mutation	p.Arg136His(p.R136H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237289
Start	137878969:137878969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368271377
CDS Mutation	c.1524C>T
Mutation Classification	Silent
Feature Type	Transcript