Colon Cancer: Gene >> TCERG1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131146518:131146518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>C
AA Mutation	p.Glu393Gln(p.E393Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131308357:131308357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524C>T
AA Mutation	p.Thr175Met(p.T175M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131166871:131166871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201159848
CDS Mutation	c.871C>T
AA Mutation	p.Arg291Trp(p.R291W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131308268:131308268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613C>A
AA Mutation	p.Pro205Thr(p.P205T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131104299:131104299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775503378
CDS Mutation	c.1451G>A
AA Mutation	p.Arg484His(p.R484H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131146619:131146619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1076A>T
AA Mutation	p.Asn359Ile(p.N359I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131098374:131098374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767965022
CDS Mutation	c.1536G>T
AA Mutation	p.Lys512Asn(p.K512N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131309176:131309176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466G>T
AA Mutation	p.Asp156Tyr(p.D156Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131116863:131116863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199911619
CDS Mutation	c.1331C>T
AA Mutation	p.Pro444Leu(p.P444L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368642
Start	131116868:131116868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376560451
CDS Mutation	c.1326G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368642
Start	131093288:131093288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369936170
CDS Mutation	c.1635C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368642
Start	131146567:131146567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761953296
CDS Mutation	c.1128C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368642
Start	131260359:131260359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138987558
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368642
Start	131098356:131098356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1554A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368642
Start	131309270:131309270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368642
Start	131260338:131260338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751877949
CDS Mutation	c.777G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000368642
Start	131098349:131098349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1561G>T
AA Mutation	p.Glu521Ter(p.E521*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000368642
Start	131104323:131104323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1427T>A
AA Mutation	p.Leu476Ter(p.L476*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368642
Start	131308382:131308383(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.498dupT
AA Mutation	p.Asn167Ter(p.N167*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000368642
Start	131308392:131308392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TCERG1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131309268:131309268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.374G>T
AA Mutation	p.Gly125Val(p.G125V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368642
Start	131166804:131166804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.938A>C
AA Mutation	p.Glu313Ala(p.E313A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript