Colon Cancer: Gene >> DYM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269445
Start	49118806:49118806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769667648
CDS Mutation	c.1684G>A
AA Mutation	p.Asp562Asn(p.D562N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269445
Start	49044179:49044179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886A>G
AA Mutation	p.Tyr629Cys(p.Y629C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269445
Start	49257058:49257058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780213256
CDS Mutation	c.1412C>T
AA Mutation	p.Ser471Leu(p.S471L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269445
Start	49286544:49286544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836C>T
AA Mutation	p.Pro279Leu(p.P279L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269445
Start	49272228:49272228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1201T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269445
Start	49044148:49044148(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1917delT
AA Mutation	p.Phe639LeufsTer81(p.F639Lfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000269445
Start	49379693:49379693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259G>T
AA Mutation	p.Glu87Ter(p.E87*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000269445
Start	49333777:49333777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571G>T
AA Mutation	p.Glu191Ter(p.E191*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000269445
Start	49118893:49118893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780873164
CDS Mutation	c.1597C>T
AA Mutation	p.Arg533Ter(p.R533*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DYM

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269445
Start	49044070:49044070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1995C>G
Mutation Classification	Silent
Feature Type	Transcript