Colon Cancer: Gene >> SERPINF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324015
Start	1745816:1745816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780632227
CDS Mutation	c.274G>A
AA Mutation	p.Asp92Asn(p.D92N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324015
Start	1754220:1754220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162G>A
AA Mutation	p.Glu388Lys(p.E388K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324015
Start	1754364:1754364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306C>A
AA Mutation	p.Pro436Thr(p.P436T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324015
Start	1754229:1754229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376458796
CDS Mutation	c.1171G>A
AA Mutation	p.Val391Met(p.V391M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324015
Start	1744999:1744999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4G>A
AA Mutation	p.Ala2Thr(p.A2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324015
Start	1747106:1747106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455G>A
AA Mutation	p.Cys152Tyr(p.C152Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324015
Start	1745718:1745718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176G>A
AA Mutation	p.Gly59Asp(p.G59D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINF2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324015
Start	1747403:1747403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.606A>C
Mutation Classification	Silent
Feature Type	Transcript