Colon Cancer: Gene >> MTRR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264668
Start	7889122:7889122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255A>G
AA Mutation	p.Thr419Ala(p.T419A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264668
Start	7878231:7878231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759336378
CDS Mutation	c.770G>A
AA Mutation	p.Arg257His(p.R257H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264668
Start	7889182:7889182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315G>A
AA Mutation	p.Asp439Asn(p.D439N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264668
Start	7889198:7889198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1331T>C
AA Mutation	p.Val444Ala(p.V444A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264668
Start	7878176:7878176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715G>A
AA Mutation	p.Val239Met(p.V239M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264668
Start	7892784:7892784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1509G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264668
Start	7889098:7889098(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1235delT
AA Mutation	p.Leu412CysfsTer157(p.L412Cfs*157)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000264668
Start	7870855:7870855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142G>T
AA Mutation	p.Glu48Ter(p.E48*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264668
Start	7895854:7895854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1757+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MTRR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264668
Start	7889128:7889128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1261G>T
AA Mutation	p.Asp421Tyr(p.D421Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264668
Start	7891405:7891405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137853062
CDS Mutation	c.1442C>T
AA Mutation	p.Ser481Leu(p.S481L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264668
Start	7892747:7892747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1472G>A
AA Mutation	p.Gly491Glu(p.G491E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264668
Start	7877965:7877965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.504G>C
Mutation Classification	Silent
Feature Type	Transcript