Colon Cancer: Gene >> SFRP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37909640:37909640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>T
AA Mutation	p.Asp278Tyr(p.D278Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37916227:37916227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311C>T
AA Mutation	p.Ala104Val(p.A104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37907636:37907636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568754305
CDS Mutation	c.884G>A
AA Mutation	p.Arg295Gln(p.R295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37916225:37916225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Cys(p.R105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37909674:37909674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.798G>C
AA Mutation	p.Met266Ile(p.M266I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37907530:37907530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.990G>T
AA Mutation	p.Lys330Asn(p.K330N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37912215:37912215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766014536
CDS Mutation	c.695G>A
AA Mutation	p.Arg232Gln(p.R232Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37916455:37916455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83G>A
AA Mutation	p.Arg28His(p.R28H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436072
Start	37916115:37916115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436072
Start	37916223:37916223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761497415
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436072
Start	37916163:37916163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436072
Start	37907557:37907557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.963T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436072
Start	37916490:37916490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776767479
CDS Mutation	c.48G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436072
Start	37907581:37907581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436072
Start	37912160:37912160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SFRP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37916225:37916225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Cys(p.R105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000436072
Start	37916171:37916171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367C>G
AA Mutation	p.Leu123Val(p.L123V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000436072
Start	37914276:37914276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755909350
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Trp(p.R177W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436072
Start	37916321:37916321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217C>T
Mutation Classification	Silent
Feature Type	Transcript