Colon Cancer: Gene >> MPEG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59211962:59211962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904G>A
AA Mutation	p.Ala302Thr(p.A302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59212420:59212420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779189349
CDS Mutation	c.446G>A
AA Mutation	p.Arg149Gln(p.R149Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59212386:59212386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480A>T
AA Mutation	p.Lys160Asn(p.K160N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59212784:59212784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377026755
CDS Mutation	c.82G>A
AA Mutation	p.Glu28Lys(p.E28K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59211170:59211170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696G>A
AA Mutation	p.Ala566Thr(p.A566T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59212312:59212312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.554A>T
AA Mutation	p.Asn185Ile(p.N185I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59212342:59212342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524T>G
AA Mutation	p.Leu175Arg(p.L175R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59211050:59211050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1816G>A
AA Mutation	p.Ala606Thr(p.A606T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361050
Start	59212827:59212827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761251581
CDS Mutation	c.39G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361050
Start	59212601:59212601(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.265delC
AA Mutation	p.Gln89ArgfsTer8(p.Q89Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MPEG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59212162:59212162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704C>T
AA Mutation	p.Ala235Val(p.A235V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59212169:59212169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Cys(p.R233C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361050
Start	59211146:59211146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1720G>C
AA Mutation	p.Val574Leu(p.V574L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361050
Start	59211279:59211279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201332555
CDS Mutation	c.1587C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000361050
Start	59212685:59212685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759351832
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Ter(p.R61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript