Colon Cancer: Gene >> FBLN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327858
Start	45533156:45533156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638C>T
AA Mutation	p.Ser213Phe(p.S213F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327858
Start	45525593:45525593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236C>T
AA Mutation	p.Ala79Val(p.A79V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327858
Start	45518754:45518754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772445995
CDS Mutation	c.152C>T
AA Mutation	p.Ser51Leu(p.S51L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327858
Start	45533835:45533835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751912120
CDS Mutation	c.721C>T
AA Mutation	p.Arg241Cys(p.R241C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327858
Start	45535241:45535241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759317468
CDS Mutation	c.826G>A
AA Mutation	p.Asp276Asn(p.D276N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327858
Start	45541361:45541361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540607391
CDS Mutation	c.1055C>T
AA Mutation	p.Thr352Met(p.T352M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327858
Start	45533154:45533154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.636C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327858
Start	45548626:45548626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1131172
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327858
Start	45527879:45527879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778833132
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327858
Start	45543459:45543459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327858
Start	45518686:45518686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754024808
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000327858
Start	45543518:45543518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313C>A
AA Mutation	p.Ser438Ter(p.S438*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FBLN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327858
Start	45541314:45541314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008G>T
AA Mutation	p.Lys336Asn(p.K336N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327858
Start	45577002:45577002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368050507
CDS Mutation	c.1866G>A
Mutation Classification	Silent
Feature Type	Transcript