Colon Cancer: Gene >> MAGEC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247452
Start	142203697:142203697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291G>T
AA Mutation	p.Gln97His(p.Q97H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247452
Start	142203567:142203567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769500609
CDS Mutation	c.421C>A
AA Mutation	p.Leu141Ile(p.L141I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247452
Start	142203471:142203471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517A>C
AA Mutation	p.Lys173Gln(p.K173Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000247452
Start	142202901:142202901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1087A>G
AA Mutation	p.Ser363Gly(p.S363G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000247452
Start	142203462:142203462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526G>T
AA Mutation	p.Asp176Tyr(p.D176Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000247452
Start	142203506:142203506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482C>A
AA Mutation	p.Pro161His(p.P161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000247452
Start	142203160:142203160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828A>C
AA Mutation	p.Lys276Asn(p.K276N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247452
Start	142203970:142203970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140435962
CDS Mutation	c.18C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247452
Start	142203811:142203811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247452
Start	142203781:142203781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.207G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAGEC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247452
Start	142203147:142203147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Gly281Arg(p.G281R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247452
Start	142203070:142203070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918T>A
AA Mutation	p.His306Gln(p.H306Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247452
Start	142203688:142203688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528011223
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247452
Start	142203160:142203160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828A>G
Mutation Classification	Silent
Feature Type	Transcript