Colon Cancer: Gene >> KHSRP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6416842:6416842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1223C>G
AA Mutation	p.Pro408Arg(p.P408R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6422411:6422411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275C>T
AA Mutation	p.Ala92Val(p.A92V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6416784:6416784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1281G>T
AA Mutation	p.Met427Ile(p.M427I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6416842:6416842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758290639
CDS Mutation	c.1223C>T
AA Mutation	p.Pro408Leu(p.P408L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6416545:6416545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1433G>T
AA Mutation	p.Arg478Leu(p.R478L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6418043:6418043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Cys(p.R306C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6416519:6416519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1459G>A
AA Mutation	p.Ala487Thr(p.A487T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6418842:6418842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Trp(p.R214W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6415241:6415241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2027C>T
AA Mutation	p.Ala676Val(p.A676V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398148
Start	6416493:6416493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769685889
CDS Mutation	c.1485C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398148
Start	6417815:6417815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555066011
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398148
Start	6415173:6415173(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2095delC
AA Mutation	p.Gln699SerfsTer24(p.Q699Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398148
Start	6415280:6415280(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1988delG
AA Mutation	p.Gly663ValfsTer60(p.G663Vfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398148
Start	6418822:6418823(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.659dupC
AA Mutation	p.Gly221ArgfsTer37(p.G221Rfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000398148
Start	6421648:6421649(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.385+1_385+2delGT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KHSRP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6416305:6416305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1591C>T
AA Mutation	p.Pro531Ser(p.P531S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398148
Start	6418018:6418018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.941G>A
AA Mutation	p.Arg314Gln(p.R314Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript