Colon Cancer: Gene >> SCRN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242059
Start	29936587:29936587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874C>T
AA Mutation	p.His292Tyr(p.H292Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242059
Start	29940715:29940715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706G>T
AA Mutation	p.Gly236Cys(p.G236C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242059
Start	29955254:29955254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266G>A
AA Mutation	p.Cys89Tyr(p.C89Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242059
Start	29936671:29936671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758841869
CDS Mutation	c.790G>A
AA Mutation	p.Gly264Arg(p.G264R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242059
Start	29940770:29940770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651G>T
AA Mutation	p.Glu217Asp(p.E217D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242059
Start	29968978:29968978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242059
Start	29940845:29940845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766739416
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242059
Start	29944020:29944020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242059
Start	29968936:29968936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242059
Start	29923985:29923986(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1216_1217delGT
AA Mutation	p.Val406Ter(p.V406*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SCRN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242059
Start	29923979:29923979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193920979
CDS Mutation	c.1223C>T
AA Mutation	p.Thr408Met(p.T408M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242059
Start	29968929:29968929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373425376
CDS Mutation	c.139G>A
AA Mutation	p.Glu47Lys(p.E47K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242059
Start	29926464:29926464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant;stop_lost
Transcription ID	ENST00000242059
Start	29923959:29923959(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1243delT
AA Mutation	p.Ter415Glu(p.*415E)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000242059
Start	29968959:29968959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109G>T
AA Mutation	p.Glu37Ter(p.E37*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript