Colon Cancer: Gene >> SCG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220478
Start	51701239:51701239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202C>A
AA Mutation	p.Pro401His(p.P401H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220478
Start	51719435:51719435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316T>C
AA Mutation	p.Phe439Ser(p.F439S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220478
Start	51692238:51692238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770A>C
AA Mutation	p.Asn257Thr(p.N257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220478
Start	51683292:51683292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255A>C
AA Mutation	p.Glu85Asp(p.E85D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220478
Start	51683399:51683399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362A>C
AA Mutation	p.Asp121Ala(p.D121A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220478
Start	51701124:51701124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087C>A
AA Mutation	p.His363Asn(p.H363N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000220478
Start	51719447:51719447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1328A>G
AA Mutation	p.Gln443Arg(p.Q443R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220478
Start	51688327:51688327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220478
Start	51683253:51683263(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.216_226delTGATAACTTGA
AA Mutation	p.Asp73ProfsTer12(p.D73Pfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000220478
Start	51683078:51683078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000220478
Start	51699404:51699404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SCG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220478
Start	51682537:51682537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103G>A
AA Mutation	p.Glu35Lys(p.E35K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220478
Start	51688396:51688396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220478
Start	51689281:51689281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript