Colon Cancer: Gene >> MDM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367182
Start	204549320:204549320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111G>A
AA Mutation	p.Val371Ile(p.V371I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367182
Start	204542943:204542943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671A>T
AA Mutation	p.Gln224Leu(p.Q224L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367182
Start	204546825:204546825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851T>C
AA Mutation	p.Leu284Pro(p.L284P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367182
Start	204538264:204538264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467C>A
AA Mutation	p.Pro156His(p.P156H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367182
Start	204542879:204542879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607T>A
AA Mutation	p.Leu203Ile(p.L203I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367182
Start	204542848:204542848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367182
Start	204544651:204544652(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.789_790insTG
AA Mutation	p.Ser264Ter(p.S264*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000367182
Start	204549672:204549673(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1463_1464insCTG
AA Mutation	p.Phe488_Ile489insCys(p.F488_I489insC)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MDM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367182
Start	204549309:204549309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201947927
CDS Mutation	c.1100C>T
AA Mutation	p.Ser367Leu(p.S367L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367182
Start	204549132:204549132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923A>C
AA Mutation	p.Glu308Ala(p.E308A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript