Colon Cancer: Gene >> ACO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216254
Start	41518537:41518537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997C>A
AA Mutation	p.His333Asn(p.H333N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216254
Start	41499856:41499856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534016929
CDS Mutation	c.167G>A
AA Mutation	p.Arg56His(p.R56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216254
Start	41511890:41511890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.447A>C
AA Mutation	p.Glu149Asp(p.E149D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216254
Start	41526443:41526443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755695367
CDS Mutation	c.1943G>A
AA Mutation	p.Arg648His(p.R648H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216254
Start	41520181:41520181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1043A>G
AA Mutation	p.His348Arg(p.H348R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216254
Start	41525259:41525259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1672G>A
AA Mutation	p.Val558Met(p.V558M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216254
Start	41526426:41526426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150391290
CDS Mutation	c.1926C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216254
Start	41527320:41527320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760073057
CDS Mutation	c.1986C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216254
Start	41520179:41520179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1041A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216254
Start	41507899:41507899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142651093
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000216254
Start	41523273:41523273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365G>A
AA Mutation	p.Trp455Ter(p.W455*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000216254
Start	41528024:41528024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2208+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ACO2

No Mutation Annotation!