Colon Cancer: Gene >> DRD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362072
Start	113412813:113412813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881G>T
AA Mutation	p.Arg294Leu(p.R294L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362072
Start	113412713:113412713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981G>T
AA Mutation	p.Lys327Asn(p.K327N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362072
Start	113424567:113424567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>A
AA Mutation	p.Ala29Thr(p.A29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362072
Start	113412804:113412804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890C>A
AA Mutation	p.Pro297His(p.P297H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000362072
Start	113410831:113410831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758683320
CDS Mutation	c.1228G>A
AA Mutation	p.Ala410Thr(p.A410T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000362072
Start	113412677:113412677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017G>T
AA Mutation	p.Lys339Asn(p.K339N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362072
Start	113410835:113410835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1224C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362072
Start	113410808:113410808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362072
Start	113424502:113424502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767660986
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362072
Start	113424457:113424457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362072
Start	113418092:113418092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201130366
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DRD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362072
Start	113410801:113410801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1258G>A
AA Mutation	p.Ala420Thr(p.A420T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362072
Start	113424502:113424502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767660986
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362072
Start	113412599:113412599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095G>A
Mutation Classification	Silent
Feature Type	Transcript