Colon Cancer: Gene >> AHCY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217426
Start	34290775:34290775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722T>C
AA Mutation	p.Ile241Thr(p.I241T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217426
Start	34285513:34285513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094A>G
AA Mutation	p.Gln365Arg(p.Q365R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217426
Start	34290782:34290782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375760628
CDS Mutation	c.715G>A
AA Mutation	p.Val239Ile(p.V239I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217426
Start	34295468:34295468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563484762
CDS Mutation	c.146G>A
AA Mutation	p.Arg49His(p.R49H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217426
Start	34285496:34285496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111G>A
AA Mutation	p.Glu371Lys(p.E371K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217426
Start	34290603:34290603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802G>C
AA Mutation	p.Glu268Gln(p.E268Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000217426
Start	34295508:34295508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106C>T
AA Mutation	p.Arg36Trp(p.R36W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000217426
Start	34295412:34295412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199533546
CDS Mutation	c.202G>A
AA Mutation	p.Val68Ile(p.V68I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217426
Start	34290861:34290861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141172613
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217426
Start	34295461:34295461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217426
Start	34292452:34292452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AHCY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217426
Start	34281071:34281071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1262G>A
AA Mutation	p.Cys421Tyr(p.C421Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript