Colon Cancer: Gene >> BACH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29326364:29326364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540G>T
AA Mutation	p.Gln180His(p.Q180H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29327331:29327331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1507G>A
AA Mutation	p.Asp503Asn(p.D503N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29329530:29329530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613G>A
AA Mutation	p.Arg538Gln(p.R538Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29326618:29326618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794G>A
AA Mutation	p.Gly265Glu(p.G265E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29327347:29327347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523C>T
AA Mutation	p.Thr508Ile(p.T508I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29321416:29321416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136C>A
AA Mutation	p.Arg46Ser(p.R46S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29326543:29326543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553355487
CDS Mutation	c.719G>A
AA Mutation	p.Arg240His(p.R240H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29327114:29327114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290G>T
AA Mutation	p.Gln430His(p.Q430H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29326633:29326633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809G>A
AA Mutation	p.Cys270Tyr(p.C270Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29326687:29326687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863C>A
AA Mutation	p.Pro288His(p.P288H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286800
Start	29342668:29342668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2046C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BACH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29329530:29329530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613G>A
AA Mutation	p.Arg538Gln(p.R538Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29326665:29326665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Glu281Lys(p.E281K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29326510:29326510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>C
AA Mutation	p.Lys229Thr(p.K229T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286800
Start	29329620:29329620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1703G>A
AA Mutation	p.Arg568Lys(p.R568K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286800
Start	29321364:29321364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84G>A
Mutation Classification	Silent
Feature Type	Transcript