Colon Cancer: Gene >> RAD17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380774
Start	69396496:69396496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1555T>A
AA Mutation	p.Ser519Thr(p.S519T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380774
Start	69384905:69384905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650G>T
AA Mutation	p.Arg217Ile(p.R217I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380774
Start	69373963:69373963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176G>A
AA Mutation	p.Ser59Asn(p.S59N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380774
Start	69389049:69389049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943A>G
AA Mutation	p.Thr315Ala(p.T315A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380774
Start	69396401:69396401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1460G>A
AA Mutation	p.Arg487His(p.R487H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380774
Start	69391903:69391903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759753593
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371Gln(p.R371Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380774
Start	69414287:69414287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2041A>G
AA Mutation	p.Thr681Ala(p.T681A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380774
Start	69414203:69414203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000380774
Start	69386199:69386199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Ter(p.R251*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380774
Start	69391906:69391907(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1122dupA
AA Mutation	p.Pro375ThrfsTer2(p.P375Tfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380774
Start	69373933:69373934(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.152dupA
AA Mutation	p.Asn51LysfsTer37(p.N51Kfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAD17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380774
Start	69384825:69384825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570G>T
AA Mutation	p.Gln190His(p.Q190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380774
Start	69414185:69414185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1939C>A
AA Mutation	p.Gln647Lys(p.Q647K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript