Colon Cancer: Gene >> TFRC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360110
Start	196051968:196051968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141165322
CDS Mutation	c.2257G>A
AA Mutation	p.Val753Ile(p.V753I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360110
Start	196072055:196072055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532C>T
AA Mutation	p.Leu178Phe(p.L178F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360110
Start	196075168:196075168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229T>G
AA Mutation	p.Phe77Val(p.F77V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360110
Start	196053521:196053521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1937G>A
AA Mutation	p.Arg646His(p.R646H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360110
Start	196055199:196055199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768871682
CDS Mutation	c.1780G>A
AA Mutation	p.Ala594Thr(p.A594T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360110
Start	196074051:196074051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773087880
CDS Mutation	c.313G>A
AA Mutation	p.Glu105Lys(p.E105K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360110
Start	196052010:196052010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2215A>G
AA Mutation	p.Thr739Ala(p.T739A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360110
Start	196074002:196074002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772641140
CDS Mutation	c.362G>A
AA Mutation	p.Arg121His(p.R121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360110
Start	196069518:196069518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360110
Start	196058299:196058299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1662T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360110
Start	196072116:196072116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360110
Start	196052038:196052038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776066581
CDS Mutation	c.2187G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000360110
Start	196052133:196052133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373764388
CDS Mutation	c.2092C>T
AA Mutation	p.Arg698Ter(p.R698*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TFRC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360110
Start	196072067:196072067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746712619
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Cys(p.R174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript