Colon Cancer: Gene >> FLCN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285071
Start	17216463:17216463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1217G>A
AA Mutation	p.Ser406Asn(p.S406N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285071
Start	17213716:17213716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1679C>T
AA Mutation	p.Thr560Ile(p.T560I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285071
Start	17215227:17215227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390G>A
AA Mutation	p.Glu464Lys(p.E464K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285071
Start	17228115:17228115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.23G>A
AA Mutation	p.Cys8Tyr(p.C8Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285071
Start	17222529:17222529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751T>A
AA Mutation	p.Trp251Arg(p.W251R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285071
Start	17213773:17213773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764899882
CDS Mutation	c.1622C>T
AA Mutation	p.Ala541Val(p.A541V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000285071
Start	17213815:17213815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1580G>C
AA Mutation	p.Arg527Pro(p.R527P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285071
Start	17216393:17216393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374707789
CDS Mutation	c.1287C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285071
Start	17216390:17216390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285071
Start	17222599:17222599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781035304
CDS Mutation	c.681G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285071
Start	17228060:17228060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746222481
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285071
Start	17222524:17222524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746664975
CDS Mutation	c.756G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000285071
Start	17216395:17216395(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs80338683
CDS Mutation	c.1285delC
AA Mutation	p.His429ThrfsTer39(p.H429Tfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000285071
Start	17216394:17216395(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs80338682
CDS Mutation	c.1285dupC
AA Mutation	p.His429ProfsTer27(p.H429Pfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FLCN

Mutation ID	1
Mutation Consequence	start_lost
Transcription ID	ENST00000285071
Start	17228135:17228135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript