Colon Cancer: Gene >> MARCH7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259050
Start	159729128:159729128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106A>G
AA Mutation	p.Thr36Ala(p.T36A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259050
Start	159743136:159743136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139916486
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Cys(p.R77C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259050
Start	159748744:159748744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778411794
CDS Mutation	c.1454G>A
AA Mutation	p.Arg485Gln(p.R485Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259050
Start	159748753:159748753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1463T>C
AA Mutation	p.Val488Ala(p.V488A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259050
Start	159729060:159729060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38C>A
AA Mutation	p.Ser13Tyr(p.S13Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000259050
Start	159729164:159729164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142T>C
AA Mutation	p.Ser48Pro(p.S48P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259050
Start	159748268:159748268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259050
Start	159747918:159747919(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.628_629insTATTTTTGAAAGGA
AA Mutation	p.Gln210LeufsTer9(p.Q210Lfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MARCH7

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000259050
Start	159764627:159764627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2009T>G
AA Mutation	p.Phe670Cys(p.F670C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000259050
Start	159729150:159729150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128C>A
AA Mutation	p.Ser43Ter(p.S43*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript