Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ACSM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289416
Start	20775859:20775859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240T>G
AA Mutation	p.Asn80Lys(p.N80K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289416
Start	20785018:20785018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054G>T
AA Mutation	p.Ala352Ser(p.A352S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289416
Start	20790663:20790663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301C>A
AA Mutation	p.Pro434Gln(p.P434Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289416
Start	20775876:20775876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.257T>C
AA Mutation	p.Ile86Thr(p.I86T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000289416
Start	20770137:20770137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103G>A
AA Mutation	p.Ala35Thr(p.A35T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289416
Start	20796951:20796951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1740G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289416
Start	20796453:20796454(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs757021642
CDS Mutation	c.1645dupA
AA Mutation	p.Thr549AsnfsTer29(p.T549Nfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ACSM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289416
Start	20781015:20781015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824C>T
AA Mutation	p.Thr275Ile(p.T275I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000289416
Start	20780975:20780975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784T>C
AA Mutation	p.Phe262Leu(p.F262L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289416
Start	20781115:20781115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757135564
CDS Mutation	c.924G>A
Mutation Classification	Silent
Feature Type	Transcript