Colon Cancer: Gene >> MLEC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228506
Start	120694114:120694114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259C>T
AA Mutation	p.Pro87Ser(p.P87S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228506
Start	120696340:120696340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758206205
CDS Mutation	c.674C>T
AA Mutation	p.Pro225Leu(p.P225L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228506
Start	120694939:120694939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.530A>C
AA Mutation	p.Lys177Thr(p.K177T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228506
Start	120694123:120694123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268C>A
AA Mutation	p.Arg90Ser(p.R90S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228506
Start	120696335:120696335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228506
Start	120687520:120687520(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.226delG
AA Mutation	p.Val76TrpfsTer9(p.V76Wfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000228506
Start	120696315:120696315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MLEC

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228506
Start	120694850:120694850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368412650
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript