Colon Cancer: Gene >> DFFA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377038
Start	10469278:10469278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197A>T
AA Mutation	p.Asp66Val(p.D66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377038
Start	10463443:10463443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619T>C
AA Mutation	p.Ser207Pro(p.S207P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377038
Start	10467196:10467196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>A
AA Mutation	p.Asp145Glu(p.D145E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377038
Start	10461614:10461614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372939210
CDS Mutation	c.872G>A
AA Mutation	p.Arg291Gln(p.R291Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377038
Start	10463191:10463191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650G>T
AA Mutation	p.Gly217Val(p.G217V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377038
Start	10472345:10472345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377038
Start	10463139:10463139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369167862
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DFFA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377038
Start	10463491:10463491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571C>A
AA Mutation	p.Leu191Ile(p.L191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377038
Start	10467210:10467210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
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	ENST00000377038
Start	10469246:10469246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229C>A
AA Mutation	p.Leu77Met(p.L77M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript