Colon Cancer: Gene >> MFN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235329
Start	12007180:12007180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2000A>C
AA Mutation	p.Glu667Ala(p.E667A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000235329
Start	11999095:11999095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816G>T
AA Mutation	p.Glu272Asp(p.E272D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235329
Start	12007116:12007116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754683866
CDS Mutation	c.1936G>A
AA Mutation	p.Val646Ile(p.V646I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000235329
Start	11996314:11996314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470C>T
AA Mutation	p.Ala157Val(p.A157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000235329
Start	12007156:12007156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1976G>T
AA Mutation	p.Arg659Met(p.R659M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000235329
Start	12001497:12001497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.913T>C
AA Mutation	p.Ser305Pro(p.S305P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000235329
Start	11989254:11989254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.86T>C
AA Mutation	p.Leu29Pro(p.L29P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235329
Start	11996210:11996210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235329
Start	11992679:11992679(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.306delT
AA Mutation	p.Phe102LeufsTer11(p.F102Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MFN2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235329
Start	12005841:12005841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1626G>A
Mutation Classification	Silent
Feature Type	Transcript