Colon Cancer: Gene >> DHCR7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355527
Start	71441270:71441270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151170252
CDS Mutation	c.583G>A
AA Mutation	p.Ala195Thr(p.A195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355527
Start	71435704:71435704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531038145
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Cys(p.R367C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355527
Start	71444862:71444862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367585401
CDS Mutation	c.91C>A
AA Mutation	p.Arg31Ser(p.R31S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355527
Start	71435518:71435518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285C>T
AA Mutation	p.Pro429Ser(p.P429S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355527
Start	71439065:71439065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773048017
CDS Mutation	c.645C>A
AA Mutation	p.Phe215Leu(p.F215L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355527
Start	71437869:71437869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80338858
CDS Mutation	c.906C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355527
Start	71444188:71444188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150928869
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355527
Start	71444167:71444167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771419549
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000355527
Start	71441359:71441361(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.492_494delCCT
AA Mutation	p.Leu165del(p.L165del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DHCR7

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000355527
Start	71439053:71439053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.657C>A
AA Mutation	p.Tyr219Ter(p.Y219*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript