Colon Cancer: Gene >> FNDC3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49203241:49203241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3239A>G
AA Mutation	p.Tyr1080Cys(p.Y1080C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49207295:49207295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200658303
CDS Mutation	c.3497G>A
AA Mutation	p.Arg1166Gln(p.R1166Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49006225:49006225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.35A>T
AA Mutation	p.Gln12Leu(p.Q12L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49145803:49145803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845T>C
AA Mutation	p.Val282Ala(p.V282A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49191364:49191364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771506910
CDS Mutation	c.2206C>T
AA Mutation	p.Arg736Cys(p.R736C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49191095:49191095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2025A>C
AA Mutation	p.Lys675Asn(p.K675N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49131302:49131302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199834112
CDS Mutation	c.418G>A
AA Mutation	p.Val140Met(p.V140M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49136419:49136419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369583924
CDS Mutation	c.578G>A
AA Mutation	p.Arg193His(p.R193H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49207151:49207151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3353T>C
AA Mutation	p.Val1118Ala(p.V1118A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000492622
Start	49191363:49191363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2205A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000492622
Start	49075318:49075318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000492622
Start	49186080:49186080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1734A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000492622
Start	49207308:49207308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145742724
CDS Mutation	c.3510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000492622
Start	49191280:49191280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2122G>T
AA Mutation	p.Glu708Ter(p.E708*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000492622
Start	49191108:49191108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2038C>T
AA Mutation	p.Gln680Ter(p.Q680*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FNDC3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000492622
Start	49198535:49198535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2948C>A
AA Mutation	p.Ser983Tyr(p.S983Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000492622
Start	49168664:49168664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1089C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000492622
Start	49131158:49131158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274C>T
AA Mutation	p.Arg92Ter(p.R92*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript