Colon Cancer: Gene >> SMOC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381280
Start	69953440:69953440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745832952
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381280
Start	70023350:70023350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1194G>T
AA Mutation	p.Lys398Asn(p.K398N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381280
Start	69952250:69952250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376548937
CDS Mutation	c.212G>A
AA Mutation	p.Arg71Gln(p.R71Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381280
Start	70011489:70011489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769420307
CDS Mutation	c.862G>A
AA Mutation	p.Val288Met(p.V288M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381280
Start	70023241:70023241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085G>T
AA Mutation	p.Arg362Leu(p.R362L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381280
Start	70010766:70010766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759730772
CDS Mutation	c.677C>T
AA Mutation	p.Ser226Leu(p.S226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381280
Start	70010922:70010922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746033223
CDS Mutation	c.833G>A
AA Mutation	p.Arg278His(p.R278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381280
Start	70011488:70011488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761319347
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381280
Start	69975753:69975753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000381280
Start	70010879:70010879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790C>T
AA Mutation	p.Gln264Ter(p.Q264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SMOC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381280
Start	69992422:69992422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763002694
CDS Mutation	c.532G>A
AA Mutation	p.Gly178Arg(p.G178R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381280
Start	69952221:69952221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381280
Start	70023311:70023311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542274320
CDS Mutation	c.1155G>A
Mutation Classification	Silent
Feature Type	Transcript