Colon Cancer: Gene >> POLH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43610608:43610608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129C>T
AA Mutation	p.Arg377Cys(p.R377C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43614342:43614342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1927C>A
AA Mutation	p.Pro643Thr(p.P643T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43610626:43610626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551944293
CDS Mutation	c.1147C>T
AA Mutation	p.Arg383Cys(p.R383C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43614066:43614066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1651T>C
AA Mutation	p.Ser551Pro(p.S551P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43597788:43597788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583G>A
AA Mutation	p.Val195Met(p.V195M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43610705:43610705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226C>A
AA Mutation	p.Ser409Tyr(p.S409Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43614153:43614153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1738G>T
AA Mutation	p.Gly580Trp(p.G580W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43614008:43614008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1593C>A
AA Mutation	p.Phe531Leu(p.F531L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43597728:43597728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523C>T
AA Mutation	p.Leu175Phe(p.L175F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372236
Start	43597838:43597838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372236
Start	43614089:43614089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1674C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372236
Start	43614534:43614534(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2124delT
AA Mutation	p.Phe708LeufsTer4(p.F708Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> POLH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372236
Start	43613764:43613764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1349C>A
AA Mutation	p.Ser450Tyr(p.S450Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript