Colon Cancer: Gene >> GATAD2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368655
Start	153813393:153813393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1276G>A
AA Mutation	p.Asp426Asn(p.D426N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368655
Start	153818087:153818087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682C>T
AA Mutation	p.Arg228Trp(p.R228W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368655
Start	153819647:153819647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424A>T
AA Mutation	p.Met142Leu(p.M142L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368655
Start	153817416:153817416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764367916
CDS Mutation	c.856C>T
AA Mutation	p.Arg286Cys(p.R286C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368655
Start	153828223:153828223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368655
Start	153818167:153818167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.602C>A
AA Mutation	p.Pro201Gln(p.P201Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368655
Start	153817471:153817471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368655
Start	153828240:153828240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368655
Start	153816373:153816373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368655
Start	153812031:153812031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753763024
CDS Mutation	c.1521G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000368655
Start	153828257:153828257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91C>T
AA Mutation	p.Arg31Ter(p.R31*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000368655
Start	153816538:153816538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951T>G
AA Mutation	p.Tyr317Ter(p.Y317*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GATAD2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368655
Start	153813447:153813447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1222A>G
AA Mutation	p.Ser408Gly(p.S408G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000368655
Start	153828257:153828257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91C>T
AA Mutation	p.Arg31Ter(p.R31*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript