Colon Cancer: Gene >> TNFRSF21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296861
Start	47253282:47253282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483C>T
AA Mutation	p.Arg495Cys(p.R495C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296861
Start	47253389:47253389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376C>T
AA Mutation	p.Ala459Val(p.A459V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296861
Start	47253495:47253495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1270G>A
AA Mutation	p.Ala424Thr(p.A424T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296861
Start	47232964:47232964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778427574
CDS Mutation	c.1769G>A
AA Mutation	p.Arg590His(p.R590H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296861
Start	47284204:47284204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766706578
CDS Mutation	c.977C>T
AA Mutation	p.Thr326Met(p.T326M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296861
Start	47253402:47253402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363G>A
AA Mutation	p.Asp455Asn(p.D455N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296861
Start	47284124:47284124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057A>G
AA Mutation	p.Met353Val(p.M353V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296861
Start	47232963:47232963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1770C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296861
Start	47284077:47284077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1104C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296861
Start	47286395:47286395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.297T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296861
Start	47309449:47309449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296861
Start	47234758:47234758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296861
Start	47284080:47284080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296861
Start	47286253:47286253(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.439delC
AA Mutation	p.His147IlefsTer37(p.H147Ifs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296861
Start	47286543:47286544(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.148_149insAA
AA Mutation	p.Leu50GlnfsTer17(p.L50Qfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296861
Start	47286544:47286545(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.147_148insTTCT
AA Mutation	p.Leu50PhefsTer10(p.L50Ffs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296861
Start	47232845:47232845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769216892
CDS Mutation	c.1888G>A
AA Mutation	p.Glu630Lys(p.E630K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript