Colon Cancer: Gene >> ACADS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242592
Start	120738374:120738374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.719A>G
AA Mutation	p.Asn240Ser(p.N240S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242592
Start	120739182:120739182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072G>A
AA Mutation	p.Ala358Thr(p.A358T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242592
Start	120738311:120738311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148588313
CDS Mutation	c.656C>T
AA Mutation	p.Thr219Met(p.T219M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242592
Start	120737008:120737008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233G>A
AA Mutation	p.Gly78Glu(p.G78E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242592
Start	120737886:120737886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143925225
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242592
Start	120737069:120737069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143169456
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242592
Start	120738369:120738369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771881207
CDS Mutation	c.714G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACADS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242592
Start	120739339:120739339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183161718
CDS Mutation	c.1130C>T
AA Mutation	p.Pro377Leu(p.P377L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242592
Start	120727138:120727138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159G>C
AA Mutation	p.Leu53Phe(p.L53F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242592
Start	120738875:120738875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199633532
CDS Mutation	c.989G>A
AA Mutation	p.Arg330His(p.R330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242592
Start	120727108:120727108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242592
Start	120727137:120727138(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.158_159insC
AA Mutation	p.Leu53PhefsTer10(p.L53Ffs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript