Colon Cancer: Gene >> NAT10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34140423:34140423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755795306
CDS Mutation	c.2443G>A
AA Mutation	p.Ala815Thr(p.A815T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34108293:34108293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68G>T
AA Mutation	p.Arg23Ile(p.R23I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34141782:34141782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2776A>G
AA Mutation	p.Met926Val(p.M926V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34136645:34136645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2032G>T
AA Mutation	p.Val678Phe(p.V678F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34130917:34130917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148211973
CDS Mutation	c.1349C>T
AA Mutation	p.Thr450Met(p.T450M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34132198:34132198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1594C>T
AA Mutation	p.Leu532Phe(p.L532F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34122501:34122501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.823A>C
AA Mutation	p.Thr275Pro(p.T275P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34118468:34118468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745G>T
AA Mutation	p.Gly249Cys(p.G249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34146156:34146156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3042G>T
AA Mutation	p.Lys1014Asn(p.K1014N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34140510:34140510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2530G>A
AA Mutation	p.Ala844Thr(p.A844T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257829
Start	34127528:34127528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141428058
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257829
Start	34132203:34132203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762435719
CDS Mutation	c.1599C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257829
Start	34112082:34112082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257829
Start	34146159:34146160(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs773784521
CDS Mutation	c.3051dupA
AA Mutation	p.Asp1018ArgfsTer19(p.D1018Rfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NAT10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34112061:34112061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210G>T
AA Mutation	p.Lys70Asn(p.K70N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257829
Start	34130917:34130917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148211973
CDS Mutation	c.1349C>T
AA Mutation	p.Thr450Met(p.T450M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript