Colon Cancer: Gene >> FBL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221801
Start	39839108:39839108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476C>G
AA Mutation	p.Pro159Arg(p.P159R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221801
Start	39834768:39834768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841T>C
AA Mutation	p.Ser281Pro(p.S281P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221801
Start	39839139:39839139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445C>A
AA Mutation	p.Leu149Met(p.L149M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221801
Start	39840737:39840737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762429726
CDS Mutation	c.61C>T
AA Mutation	p.Arg21Cys(p.R21C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221801
Start	39840491:39840491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206A>T
AA Mutation	p.Asn69Ile(p.N69I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221801
Start	39840704:39840704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749288592
CDS Mutation	c.94G>A
AA Mutation	p.Gly32Arg(p.G32R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000221801
Start	39840428:39840428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201617067
CDS Mutation	c.269C>T
AA Mutation	p.Pro90Leu(p.P90L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000221801
Start	39834544:39834544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960G>T
AA Mutation	p.Lys320Asn(p.K320N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000221801
Start	39837830:39837830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149587207
CDS Mutation	c.563A>G
AA Mutation	p.Tyr188Cys(p.Y188C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221801
Start	39839101:39839101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221801
Start	39834682:39834682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221801
Start	39834553:39834553(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.951delC
AA Mutation	p.Lys318ArgfsTer2(p.K318Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000221801
Start	39840755:39840755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43C>T
AA Mutation	p.Arg15Ter(p.R15*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FBL

No Mutation Annotation!