Colon Cancer: Gene >> ACSS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34913148:34913148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427G>A
AA Mutation	p.Val143Ile(p.V143I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34921797:34921797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1479C>A
AA Mutation	p.Phe493Leu(p.F493L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34927102:34927102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1994G>T
AA Mutation	p.Arg665Leu(p.R665L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34913443:34913443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517C>A
AA Mutation	p.Leu173Ile(p.L173I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34923387:34923387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1613C>G
AA Mutation	p.Thr538Arg(p.T538R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34925706:34925706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774600970
CDS Mutation	c.1666C>T
AA Mutation	p.Arg556Trp(p.R556W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34913175:34913175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454C>A
AA Mutation	p.Leu152Ile(p.L152I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34923374:34923374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754546126
CDS Mutation	c.1600G>A
AA Mutation	p.Glu534Lys(p.E534K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34882944:34882944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757812388
CDS Mutation	c.329G>A
AA Mutation	p.Arg110Gln(p.R110Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360596
Start	34921821:34921821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1503G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360596
Start	34921032:34921032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760720132
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360596
Start	34914403:34914403(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs756048003
CDS Mutation	c.806delC
AA Mutation	p.Pro269GlnfsTer69(p.P269Qfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360596
Start	34913112:34913112(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.394delG
AA Mutation	p.Glu132ArgfsTer38(p.E132Rfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360596
Start	34923327:34923334(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1553_1560delTCAAGCAG
AA Mutation	p.Phe518SerfsTer17(p.F518Sfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000360596
Start	34926882:34926882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909G>T
AA Mutation	p.Glu637Ter(p.E637*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000360596
Start	34921444:34921446(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1394_1396delTCT
AA Mutation	p.Phe465del(p.F465del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ACSS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360596
Start	34921596:34921596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1463C>A
AA Mutation	p.Ser488Tyr(p.S488Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript