Colon Cancer: Gene >> CASP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000432109
Start	201285047:201285047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1034G>T
AA Mutation	p.Cys345Phe(p.C345F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000432109
Start	201284972:201284972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.959A>G
AA Mutation	p.Lys320Arg(p.K320R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000432109
Start	201285137:201285137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124C>T
AA Mutation	p.Ser375Leu(p.S375L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000432109
Start	201285242:201285242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1229T>C
AA Mutation	p.Val410Ala(p.V410A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000432109
Start	201266704:201266704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218A>C
AA Mutation	p.Asp73Ala(p.D73A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000432109
Start	201286463:201286463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746684914
CDS Mutation	c.1309G>A
AA Mutation	p.Asp437Asn(p.D437N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432109
Start	201276859:201276859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.693A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432109
Start	201266579:201266579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772151801
CDS Mutation	c.93G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000432109
Start	201286567:201286567(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1419delA
AA Mutation	p.Lys473AsnfsTer?(p.K473Nfs*?)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000432109
Start	201276864:201276864(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.701delG
AA Mutation	p.Gly234AspfsTer4(p.G234Dfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000432109
Start	201285076:201285076(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1068delT
AA Mutation	p.Phe356LeufsTer26(p.F356Lfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000432109
Start	201285292:201285292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1279C>T
AA Mutation	p.Gln427Ter(p.Q427*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000432109
Start	201266510:201266510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24T>A
AA Mutation	p.Tyr8Ter(p.Y8*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000432109
Start	201272764:201272764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.538G>T
AA Mutation	p.Glu180Ter(p.E180*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000432109
Start	201284910:201284910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897C>A
AA Mutation	p.Tyr299Ter(p.Y299*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000432109
Start	201285307:201285307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1294C>T
AA Mutation	p.Arg432Ter(p.R432*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000432109
Start	201285157:201285157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144G>T
AA Mutation	p.Glu382Ter(p.E382*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000432109
Start	201285075:201285076(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1068dupT
AA Mutation	p.Ile357TyrfsTer8(p.I357Yfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000432109
Start	201286530:201286531(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1380dupG
AA Mutation	p.Lys461GlufsTer19(p.K461Efs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000432109
Start	201274902:201274903(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.613dupG
AA Mutation	p.Val205GlyfsTer13(p.V205Gfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CASP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000432109
Start	201272725:201272725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499A>C
AA Mutation	p.Ile167Leu(p.I167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000432109
Start	201271556:201271556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346G>T
AA Mutation	p.Glu116Ter(p.E116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript